Syrup & Suspension
Offering you a complete choice of products which include artemether & lumefantrine for oral suspension, carbocisteine syrup 2%, erythromycin stearate for oral suspension, azithromycin for oral suspension usp 200mg/5ml and benzyl benzoate application bp cutaneous emulsion.Artemether & Lumefantrine For Oral Suspension
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Product Details:| Usage/Application | Clinical |
| Dose | As directed by the Physician. |
| Packaging Size | 60 ml |
| Brand | DEVARTEM-DS |
| Packaging Type | Bottle |
| Product Type | Finished Product |
DEVARTEM-DS
Artemether & Lumefantrine For Oral Suspension
Composition :
Each 5 ml (after reconstituted) contains :
Artemether ....................................... 20 mg
Lumefantrine ..................................120 mg
Excipients ............................................. q.s.
Colour : Erythrosine
Indications :
Artemether / Lumefantrine is indicated for the treatment of uncomplicated P.falciparum malaria including multi-drug resistant strains of P.falciparum. Artemether and Lumefantrine for oral suspension is also effective against the blood stage of P.vivax but not active against hypozoites Artemether / Lumefantrine must be used for the malaria infections acquired in areas where the parasites may be resistant to other anti-malarial drugs.
Presentation : 60ml Bottle in printed carton with pack insert.
Additional Information:
- Item Code: L008
- Packaging Details: 60ml HDPE Bottle in printed carton with pack insert.
Artemether & Lumefantrine For Oral Suspension
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Product Details:| Packaging Size | 60 ml with Syringe + WFI (50ml). |
| Brand | DEVARTEM DS PLUS |
| Manufacturer | DEVLIFE CORPORATION PVT. LTD. |
| Composition | Artemether and lumefantrine |
| Treatment | Antimalarial |
| Prescription/Non prescription | Prescription |
| Form | Syrup |
| Shelf life | 2 Years |
| Country of Origin | Made in India |
| Strength | 180 + 1080 mg |
| Dosage Form | Powder for Oral Suspension |
ACTIVE INGREDIENTS:
Artemether and lumefantrine PRESENTATION:ARTEMETHER+LUMEFANTRINE FOR ORAL SUSPENSION(Artemether 180 mg + Lumefantrine 1080mg in 60 ml)
INDICATIONS:
ARTEMETHER+LUMEFANTRINE FOR ORAL SUSPENSION is indicated for the treatment of malaria in children caused by all forms of plasmodium including severe malaria caused by multiple drug resistant strains of P. falciparum.
Dosage and administration
Body Weight Number of mililiters 1 st Day 2nd Day 3rd Day
5 Kgs 7 ml 7 ml 7 ml
7.5 Kgs 10 ml 10 ml 10 ml
10 Kgs 14 ml 14 ml 14 ml
15 Kgs 20 ml 20 ml 20 ml
Specification : Used in ;
- uncomplicated P.falciparum malaria including multi-drug resistant strains of P.falciparum
- malaria infections acquired in areas where the parasites may be resistant to other anti-malarial drugs
Additional Information:
- Packaging Details: 60 ml Bottle in printed carton with pack insert.
Artemether & Lumefantrine For Oral Suspension
Product Price :Get Latest Price
Product Details:| Packaging Size | 60 ml |
| Brand | DEVARTEM DS PLUS 180/1080 |
| Manufacturer | DEVLIFE CORPORATION PVT. LTD. |
| Composition | Each 5 ml contains: |
| Treatment | Antimalarial |
| Prescription/Non prescription | Prescription |
| Form | ORAL SUSPENSION |
| Shelf life | 2 Years |
| Strength | 180 + 1080 mg |
ACTIVE INGREDIENTS:
Artemether and lumefantrine PRESENTATION:ARTEMETHER+LUMEFANTRINE FOR ORAL SUSPENSION(Artemether 180 mg + Lumefantrine 1080 mg in 60 ml)
INDICATIONS:
ARTEMETHER+LUMEFANTRINE FOR ORAL SUSPENSION is indicated for the treatment of malaria in children caused by all forms of plasmodium including severe malaria caused by multiple drug resistant strains of P. falciparum.
Dosage and administration
Body Weight Number of mililiters 1 st Day 2nd Day 3rd Day
5 Kgs 7 ml 7 ml 7 ml
7.5 Kgs 10 ml 10 ml 10 ml
10 Kgs 14 ml 14 ml 14 ml
15 Kgs 20 ml 20 ml 20 ml
Specification : Used in ;
- uncomplicated P.falciparum malaria including multi-drug resistant strains of P.falciparum
- malaria infections acquired in areas where the parasites may be resistant to other anti-malarial drugs
Additional Information:
- Packaging Details: 60 ml Bottle in printed carton with pack insert.
Carbocisteine Syrup 2%
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Product Details:| Brand | DEVCARB 2% |
| Bottle Type | AMBER PET |
| Usage/Application | Respiratory Tract Disorders |
| Bottle Size | 125 ml |
| Form | SYRUP |
| Packaging Size | 125 ml Bottle |
| Type Of Cough Syrup | Allopathic |
| Strength | 200mg / 10ml |
| Treatment | Mucolytic Agent |
| Shelf Life | 3 Years |
Each 10 ml contains
Carbocisteine BP ............... .200 mg Flavoured Syrupy Base .............. q.s. Colour: Caramel
Indications:
Carbocisteine is a mucolytic agent for the adjunctive therapy of respiratory tract disorders characterised by excessive, viscous mucus including chronic obstructive airways disease.
Dosage & Administration:
Children:
Children aged 2 to 5 years: One 5 mL measuring spoon twice a day
Children aged over 5 years: One 5 mL measuring spoon thrice a day
Specification :
Adjunctive therapy of respiratory tract disorders characterised by excessive, viscous mucus including chronic obstructive airways disease.
Additional Information:
- Packaging Details: 125 ml Bottle in printed carton with pack insert.
Erythromycin Stearate For Oral Suspension
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Product Details:| Brand | ERYSTY DS |
| Packaging Size | 100 ml |
| Form | ORAL SUSPENSION |
| Composition | Erythromycin Stearate USP Eq. to Erythromycin 125 mg |
| Manufacturer | DEVLIFE CORPORATION PVT. LTD. |
| Also gives | Third Party Manufacturing |
| Treatment | Macrolide Antibiotics |
| Shelf life | 3 Years |
| Prescription/Non prescription | Prescription |
| Dosage Form | Powder for Oral Suspension |
Composition:
Each 5 ml of reconstituted suspension contains :Erythromycin Stearate USP Eq. to Erythromycin .................. 125 mgExcipients ........................................ q.s.Colour : Erythrosine
Indications:
• Upper respiratory tract infections of mild to moderate degree caused by Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenza• Lower-respiratory tract infections of mild to moderate severity caused by Streptococcus pneumoniae or Streptococcus pyogenes• Listeriosis caused by Listeria monocytogenes• Skin and skin structure infections of mild to moderate severity caused by Streptococcus pyogenes or Staphylococcus aureus• Diphtheria: Infections due to Corynebacterium diphtheriae, as an adjunct to antitoxin, to prevent establishment of carriers and to eradicate the organism in carriers• Erythromycins are indicated for the treatment of the following infections caused by Chlamydia trachomatis : conjunctivitis of the new born, pneumonia of infancy, and urogenital infections during pregnancy. When tetracyclines are contraindicated or not tolerated.
Dosage & Administration: ChildrenAge, weight and severity of the infection are important factors in determining the proper dosage. In mild to moderate infections theusual dosage of erythromycin for children is 30 to 50 mg/kg/day in equally divided doses every 6 hours. For more severe infections this dosage may be doubled. If twice-a-day dosage is desired, one-half of the total daily dose may be given every 12 hours. Doses may also be given three times daily by administering one-third of the total daily dose every 8 hours.Adults400 mg erythromycin every 6 hours is the usual dose. Dosage may be increased up to 4 g per day according to the severity of the infection. If twice-a-day dosage is desired, one-half of the total daily dose may be given every 12 hours. Doses may also be given three times daily by administering one-third of the total daily dose every 8 hours.
Specification :
Used for ;
Upper respiratory tract infections
Lower-respiratory tract infections
Infection Due to Bordetella pertussis & Listeriosis monocytogenes.
Skin and skin structure infections
Diphtheria
Additional Information:
- Packaging Details: 100 ml Bottle in printed carton with pack insert.
Erythromycin Stearate For Oral Suspension
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Product Details:| Brand | ERYSTY DS PLUS |
| Packaging Size | 100 ml |
| Form | ORAL SUSPENSION |
| Composition | Each 5 ml of reconstituted suspension contains : |
| Manufacturer | DEVLIFE CORPORATION PVT. LTD. |
| Also gives | Third Party Manufacturing |
| Treatment | Macrolide Antibiotics |
| Shelf life | 3 Years |
| Prescription/Non prescription | Prescription |
| Dosage Form | Powder for Oral Suspension |
Composition:Each 5 ml of reconstituted suspension contains :Erythromycin Stearate USP Eq. to Erythromycin .................. 250 mgExcipients ........................................ q.s.Colour : Erythrosine
Indications:
• Upper respiratory tract infections of mild to moderate degree caused by Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenza• Lower-respiratory tract infections of mild to moderate severity caused by Streptococcus pneumoniae or Streptococcus pyogenes• Listeriosis caused by Listeria monocytogenes• Skinand skin structure infections of mild to moderate severity caused by Streptococcus pyogenes or Staphylococcus aureus• Diphtheria: Infections due to Corynebacterium diphtheriae, as an adjunct to antitoxin, to prevent establishment of carriers and toeradicate the organism in carriers• Erythromycins are indicated for the treatment of the following infections caused by Chlamydia trachomatis : conjunctivitis of thenewborn, pneumonia of infancy, and urogenital infections during pregnancy. When tetracyclines are contraindicated or not tolerated.
Dosage & Administration: ChildrenAge, weight and severity of the infection are important factors in determining the proper dosage. In mild to moderate infections theusual dosage of erythromycin for children is 30 to 50 mg/kg/day in equally divided doses every 6 hours. For more severe infections this dosage may be doubled. If twice-a-day dosage is desired, one-half of the total daily dose may be given every 12 hours. Doses may also be given three times daily by administering one-third of the total daily dose every 8 hours.Adults400 mg erythromycin every 6 hours is the usual dose. Dosage may be increased up to 4 g per day according to the severity of the infection. If twice-a-day dosage is desired, one-half of the total daily dose may be given every 12 hours. Doses may also be given three times daily by administering one-third of the total daily dose every 8 hours.
Specification :
Used for ;
Upper respiratory tract infections
Lower-respiratory tract infections
Infection Due to Bordetella pertussis & Listeriosis monocytogenes.
Skin and skin structure infections
Diphtheria
Additional Information:
- Packaging Details: 100 ml Bottle in printed carton with pack insert.
Azithromycin For Oral Suspension USP 200mg/5ml
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Product Details:| Packaging Size | 15 ml |
| Composition | Azithromycin (as Dihydrate) USP Eq. to Azithromycin base 200mg |
| Manufactured By | DEVLIFE CORPORATION PVT. LTD. |
| Usage/Application | Commercial |
| Product Type | Finished Product |
| Dose | As directed by the Physician |
| Brand | DEVAZY |
| Form | ORAL SUSPENSION |
| Strength | 200mg / 5ml |
| Shelf Life | 3 Years |
| Treatment | Macrolide Antibiotics |
Each 5ml of reconstituted suspension contains:
Azithromycin (as Dihydrate) USP
Eq. to Azithromycin base ………. 200mg
Excipients …………………………… q.s.
Colour: Tatrazine
INDICATION:
Azithromycin powder for oral suspension is indicated for the treatment of the following infections, when caused by microorganisms sensitive to azithromycin.
- acute bacterial sinusitis (adequately diagnosed)
- acute bacterial otitis media (adequately diagnosed)
- pharyngitis, tonsillitis
- acute exacerbation of chronic bronchitis (adequately diagnosed)
- mild to moderately severe community acquired pneumonia
- skin and soft tissue infections
Specification :
Treatment of the following infections, when caused by microorganisms sensitive to azithromycin.
- acute bacterial sinusitis (adequately diagnosed)
- acute bacterial otitis media (adequately diagnosed)
- pharyngitis, tonsillitis
- acute exacerbation of chronic bronchitis (adequately diagnosed)
- mild to moderately severe community acquired pneumonia
- skin and soft tissue infections
Additional Information:
- Packaging Details: 15 ml Bottle in printed carton with pack insert.
Benzyl Benzoate Application BP Cutaneous Emulsion
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Product Details:| Packaging Size | 100 ml |
| Packaging Type | Bottle |
| Brand | SARIPAL SOLUCION |
| Dose/Strength | 25% w/v |
| Storage Condition | Store in a cool & dry place. Protect from light. For external use only. shake well before use. |
Benzyl Benzoate BP ............... 25% w/v
(In Emulsifying Base)
Purified Water BP ........................... q.s.
Indications:
Benzyl benzoate is used in the topical treatment of pediculosis caused by Pediculus capitis and Phthirus pubis.
Benzyl benzoate is used in the topical treatment of scabies caused by the Sarcoptes scabiei mite.
Dosage & Administration:
Usual adult and adolescent dose
Pediculosis Topical, one application to the affected areas as a 25% emulsion; emulsion should remain on the affected areas for twenty-four hours. Treatment may be repeated two or three times, if necessary, for severe infestation.
Scabies
Topical, one application to the entire body except the head and face as a 25% emulsion, which should remain for twenty-four hours. Treatment may be repeated anytime within five days if necessary. Alternatively, the emulsion may be applied three times at twelve-hour intervals.
Additional Information:
- Packaging Details: 100 ml Bottle in a printed carton with pack insert.
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