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Each uncoated chewable tablet contains:
Albendazole USP..................400mg
Excipients............................q.s
Colour: Sunset Yellow FCF

INDICATION:
Anthelmintics.
ANTHEL is indicated in the treatment of single or mixed intestinal parasites. Clinical studies have shown alben effective in the treatment of Ascaris lumbricoides (roundworm), Trichuris trichiura (whipworm), Enterobius vermicularis (pinworm/threadworm), Ancylostoma duodenale and Necator americanus (hookworm), Taenia spp. (tapeworm) and Strongyloides stercoralis. ANTHEL has been shown to be effective in the treatment of Giardia (duodenalis or intestinalis or lamblia) infections in children.

DOSAGE AND ADMINISTRATION:
Adults and children over 2 years of age: 400 mg as a single dose in cases of Enterobius vermicularis, trichiurasis, ascariasis, hookworm and pinworm infections. The tablet may be chewed, swallowed or crushed and mixed with food. No specific procedures such as fasting or purging are required.

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• Packaging Details: 1 Tablets in printed carton with pack insert.

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Each hard gelatin capsule contains:
Azithromycin USP (As Dihydrate)
Eq. to Azithromycin (Anhydrous) .... 500 mg
Excipients ........................................... q.s.
Approved colour used in capsule shell.

INDICATIONS:
Azithromycin Capsules are indicated in the treatment of the following infections:
Acute Bacterial Sinusitis, Acute Bacterial Otitis Media, Pharyngitis, Tonsillitis, Acute exacerabation of Chronic Bronchitis, Mild to moderately severe community acquired pneumonia, skin and soft tissue infections, uncomplicated Chlamydia trachomatis urethritis and cervicitis

 
DOSAGE & ADMINISTRATION:
Adults and Elderly
For uncomplicated Chlamydia Trachomatis urethritis and cervicitis: 1000 mg as a single oral dose
For all other indications: 1500 mg; to be administered as 500 mg per day for three consecutive days
Pediatric Population
Azithromycin capsules should only be administered to children weighing more than 45 kg when normal adult dose should be used. For children under 45 kg other pharmaceutical forms of azithromycin, e.g. suspensions, may be used.

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• Packaging Details: 1x3 Capsules in printed carton with pack insert.

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Each uncoated tablet contains:
Senna extract eq. to .............. 15 mg of
Sennosides A and B as Calcium salt

INDICATION:
For short term relief of occasional constipation. This medicine does not help with weight loss.

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Each uncoated tablet contains:

Carbimazole BP.........................5mg

Excipients...............................q.s

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Each uncoated tablet contains:
Carbimazole BP ……………… 20 mg
Excipients ………………………… q.s.

Indication:
Carbimazole is indicated in the treatment of following conditions: Hyperthyroidism, Thyroidectomy in hyperthyroidism and therapy prior to and post radio-iodine treatment

 Dosage and Administration:

Adults and Elderly: The initial dose is in the range of 20 mg – 60 mg, taken in 2 – 3 divided doses. The dose should be titrated against thyroid function until the patient is euthyroid in order to reduce the risk of over treatment and resultant hypothyroidism

Pediatric Population (3 to 17 years of age): The usual initial daily dose is 15 mg per day. Use of Carbimazole in children below 2 years of age is therefore not recommended

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• Packaging Details: 10 x 10 Tablets in printed carton with pack insert.

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Each uncoated tablet contains:
Carbimazole BP ……………… 5 mg
Excipients ………………………… q.s.

Indication:
Carbimazole is indicated in the treatment of following conditions: Hyperthyroidism, Thyroidectomy in hyperthyroidism and therapy prior to and post radio-iodine treatment

Dosage and Administration:

Adults and Elderly: The initial dose is in the range of 20 mg – 60 mg, taken in 2 – 3 divided doses. The dose should be titrated against thyroid function until the patient is euthyroid in order to reduce the risk of over treatment and resultant hypothyroidism

Pediatric Population (3 to 17 years of age): The usual initial daily dose is 15 mg per day. Use of Carbimazole in children below 2 years of age is therefore not recommended

Additional Information:

• Packaging Details: 10 x 10 Tablets in printed carton with pack insert.

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Each uncoated tablet contains:              Trimethoprim BP              80 mg Sulfamethoxazole BP      400 mg
Excipients  q.s. 

INDICATION:
Co-trimoxazole tablets are indicated for the treatment of the following infections when owing to sensitive organisms:

- Treatment and prevention of Pneumocystis jiroveci (P. carinii) pneumonitis.

- Treatment and prophylaxis of toxoplasmosis

- Treatment of nocardiosis.

The following infections may be treated with co-trimoxazole where there is bacterial evidence of sensitivity to co-trimoxazole and good reason to prefer the combination of antibiotics in co-trimoxazole to a single antibiotic:

- Acute uncomplicated urinary tract infection

- Acute otitis media

- Acute exacerbation of chronic bronchitis

Consideration should be given to official guidance on the appropriate use of antibacterial agents.

DOSAGE AND ADMINISTRATION:

It may be preferable to take co-trimoxazole with some food or drink to minimise the possibility of gastrointestinal disturbances.

Standard dosage recommendations for acute infections 

Adults and children over 12 years:

This dosage approximates to 6 mg trimethoprim and 30 mg sulfamethoxazole per kilogram body weight per 24 hours.

Treatment should be continued until the patient has been symptom free for two days; the majority will require treatment for at least 5 days. If clinical improvement is not evident after 7 days therapy, the patient should be reassessed.

As an alternative to Standard Dosage for acute uncomplicated lower urinary tract infections, short-term therapy of 1 to 3 days duration has been shown to be effective.

Impaired hepatic function:

No data are available relating to dosage in patients with impaired hepatic function.

Special Dosage Recommendations

Where dosage is expressed as "tablets" this refers to the adult tablet, i.e. 80 mg Trimethoprim BP and 400 mg Sulfamethoxazole BP. If other formulations are to be used appropriate adjustment should be made.

Impaired renal function:

Adults and children over 12 years (no information is available for children under 12 years of age)

Specification : indicated for

- Treatment and prevention of Pneumocystis jiroveci (P. carinii) pneumonitis.

- Treatment and prophylaxis of toxoplasmosis

- Treatment of nocardiosis.

- Acute uncomplicated urinary tract infection

- Acute otitis media

- Acute exacerbation of chronic bronchitis

Additional Information:

• Packaging Details: 10 x 10 Tablets in printed carton with pack insert.

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Specification : used to treat:
· chest infections
·  throat or nose infections
·  ear infections
·  skin and soft tissue infections
·  heart infections
·  bones and joints infection
·  meningitis
·  digestive system infections
·  blood infections
·  kidney, bladder or the urethra (the tube which carries urine from the bladder) infections

Additional Information:

• Packaging Details: 100 ml Bottle In printed carton with pack insert.

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Each hard gelatin capsule contains
Fluconazole USP        200 mg
Excipients                   q.s.
Approved color used in empty capsule shell         

Indications:
Fluconazole Capsules are indicated for the treatment of candidal vaginitis, acute or recurrent. It can also be used for treatment of partners with associated candidal balantis

Dosage & Administration:

Adults

One Capsule daily

Children

Paediatric use is not recommended

Elderly

Not recommended in patients over 60 years

Renal Impairment

There is no separate dosing schedule in patients with renal impairment for single dose therapy.

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• Packaging Details: 1 Capsules in printed carton with pack insert.

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Each 5ml contains:
Terbutaline Sulphate BP..........1.25mg
Ambroxol Hydrochloride BP.....15mg
Guaifenesin BP...........................50mg
Flavoured Syrupy Base....................q.s
Colour: Tartrazine Supra & Brilliant Blue FCF

INDICATION:
KOFFOVIN-S is indicated for clinical relief of cough associated with bronchitis, bronchial asthma, emphysema and other bronchopulmonary disorders   where bronchospasm, mucous plugging and problems of expectoration co-exist

DOSAGE AND ADMINISTRATION:
KOFFOVIN-S is administered within 30 minutes after meal. The drug can be diluted with water or fruit juice. 
KOFFOVIN-S is prescribed:
To children aged 8 to 12 years – 2.5 ml thrice daily,
To adults – 5-10 ml thrice daily. The course duration is indicated by doctor.

Additional Information:

• Packaging Details: 100 ml bottle in printed carton with pack insert.

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Each film coated tablet contains:
Levofloxacin Hemihydrate USP
Eq. to Levofloxacin .............. 500 mg
Excipients ......................................... q.s.
Colour: Red Oxide of Iron & Titanium Dioxide USP

INDICATION:
Levofloxacin Tablets is indicated in adults for the treatment of the following infections.
• Acute bacterial sinusitis.
• Acute exacerbations of chronic bronchitis.
• Community-acquired pneumonia.
• Complicated skin and soft tissue infections

DOSAGE AND ADMINISTRATION:
Levofloxacin Tablets are administered once or twice daily. The dosage depends on the type and severity of the infection and the sensitivity of the presumed causative pathogen.
The recommended dose is 500mg-1000mg max for a maximum period of upto 10-14 days.   

Additional Information:

• Packaging Details: 1 x 10 Tablets in printed carton with pack insert.

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Each vial contains:
Omeprazole Sodium (Lyophilized)
Equivalent to Omeprazole ......... 40 mg

Indications:

Omeprazole for Injection belongs to a group of medicines called proton pump inhibitors. It works by decreasing the amount of acid made by the stomach. It helps reduce the pain and also allows the ulcer to heal Omeprazole Powder for Injection is used to treat and help heal peptic ulcers. It is also a treatment for gastroesophageal reflux disease, laryngopharyngeal reflux (LPR), and Zollinger-Ellison syndrome.

Dosage & Administration:
Alternative to oral therapy
In patients where the use of oral medicinal products is inappropriate, Omeprazole Injection 40 mg once daily is recommended. In patients with Zollinger-Ellison Syndrome the recommended initial dose of Omeprazole Injection given intravenously is 60 mg daily. Higher daily doses may be required, and the dose should be adjusted individually. When doses exceed 60 mg daily, the dose should be divided and given twice daily.
Special populations
Impaired renal function
Dose adjustment is not needed in patients with impaired renal function
Impaired hepatic function
In patients with impaired hepatic function a daily dose of 10-20 mg may be sufficient
Elderly (> 65 years old)
Dose adjustment is not needed in the elderly
Paediatric patients
There is limited experience with Omeprazole Injection for use in children.

Additional Information:

• Packaging Details: 40 mg Powder in a Vial with 10ml WFI with Pack Insert.

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Each ml contains:
Ondansetron Hydrochloride Dihydrate BP
Eq. to Ondansetron ......................... 2 mg
Water for Injection BP ....................... q.s.

 
INDICATIONS:

Ondansetron Injection is indicated for the prevention of nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy, including high-dose cisplatin.

Ondansetron Injection is indicated for the prevention of postoperative nausea and/or vomiting. As with other antiemetics, routine prophylaxis is not recommended for patients in whom there is little expectation that nausea and/or vomiting will occur postoperatively

 
DOSAGE & ADMINISTRATION :

The recommended adult intravenous dosage of Ondansetron Injection is three 0.15-mg/kg doses up to a maximum of 16 mg per dose. The first dose is infused over 15 minutes beginning 30 minutes before the start of emetogenic chemotherapy. Subsequent doses are administered 4 and 8 hours after the first dose of Ondansetron Injection.

For pediatric patients 6 months through 18 years of age, the intravenous dosage of Ondansetron Injection is three 0.15-mg/kg doses up to a maximum of 16 mg per dose.

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• Packaging Details: 2ml Ampoules in printed carton with pack insert.

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Each ml contains :
Hydroxide Polimaltose Iron (III) eq to
Elemental Iron ..................................... 20 mg
Vitamin A BP ..................................... 4000 IU
Vitamin D3 BP .................................... 400 IU
Vitamin B1 BP ....................................... 1 mg
Vitamin B2 BP .................................... 0.4 mg
Nicotinamide BP ................................... 5 mg
Flavoured Syrupy Base ........................... q.s.
Appropriate overages of Vitamins are added to compensate loss on storage.

INDICATION:
Supplementation of the diet with vitamins A, D3, B1, B2, B3 & Iron
Prophylaxis & treatment of anemia

DOSAGE & ADMINISTRATION:
Dosage for Prophylaxis of anemia
Infant : 1month to 6 months - 0.25 ml per day
7 months up to 1 year - 0.5 ml per day
Children : 1 to 3 years as directed by the Physician.
Dosage for Treatment of Anemia.
Infant : 1 month to 6 month - 0.5 ml two to three times per day.
7 months up to 1 year - 1.0 ml two or three times per day.
Children : 1 to 3 years as directed by the Physician.

Additional Information:

• Packaging Details: 30ml Bottle with Dropper in printed carton with pack insert.

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Composition :
Salicylic acid BP …. 2% w/w
Vitamin E acetate …. 1%w/w
(Alpha Tocopheryl Acetate BP)
Ointment Base …. q.s.

INDICATION:
For the treatment of hyperkeratotic and scaling conditions such as psoriasis, dry, rough, scaly, itchy skin and minor skin irritations

DOSAGE AND ADMINISTRATION:
Topical.
Recommended dose and dosage schedule
Adults, children and the elderly: apply twice daily to the affected area.

Additional Information:

• Packaging Details: 10 x 30 g ointment in printed carton with pack insert.