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Amoxicillin - 0093-4160-76 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 0093-4160
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 200    mg/5mL & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 0093-4160
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065119
Marketing Category: ANDA
Start Marketing Date: 20030402

Package Information of Amoxicillin

Package NDC: 0093-4160-76
Package Description: 50 mL in 1 BOTTLE (0093-4160-76)

NDC Information of Amoxicillin

NDC Code 0093-4160-76
Proprietary Name Amoxicillin
Package Description 50 mL in 1 BOTTLE (0093-4160-76)
Product NDC 0093-4160
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20030402
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AMOXICILLIN
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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