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Amoxicillin - 0093-3107-01 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 0093-3107
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 250    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 0093-3107
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061926
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Amoxicillin

Package NDC: 0093-3107-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-3107-01)

NDC Information of Amoxicillin

NDC Code 0093-3107-01
Proprietary Name Amoxicillin
Package Description 100 CAPSULE in 1 BOTTLE (0093-3107-01)
Product NDC 0093-3107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AMOXICILLIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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