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AMOXICILLIN - 12634-185-91 - (AMOXICILLIN)

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Drug Information of AMOXICILLIN

Product NDC: 12634-185
Proprietary Name: AMOXICILLIN
Non Proprietary Name: AMOXICILLIN
Active Ingredient(s): 500    mg/1 & nbsp;   AMOXICILLIN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of AMOXICILLIN

Product NDC: 12634-185
Labeler Name: Apotheca Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065271
Marketing Category: ANDA
Start Marketing Date: 20050308

Package Information of AMOXICILLIN

Package NDC: 12634-185-91
Package Description: 1 CAPSULE in 1 BLISTER PACK (12634-185-91)

NDC Information of AMOXICILLIN

NDC Code 12634-185-91
Proprietary Name AMOXICILLIN
Package Description 1 CAPSULE in 1 BLISTER PACK (12634-185-91)
Product NDC 12634-185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMOXICILLIN
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050308
Marketing Category Name ANDA
Labeler Name Apotheca Inc.
Substance Name AMOXICILLIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of AMOXICILLIN


General Information