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Amoxicillin - 67253-142-10 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 67253-142
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 25    mg/mL & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 67253-142
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062927
Marketing Category: ANDA
Start Marketing Date: 19881125

Package Information of Amoxicillin

Package NDC: 67253-142-10
Package Description: 100 mL in 1 BOTTLE (67253-142-10)

NDC Information of Amoxicillin

NDC Code 67253-142-10
Proprietary Name Amoxicillin
Package Description 100 mL in 1 BOTTLE (67253-142-10)
Product NDC 67253-142
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19881125
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
Substance Name AMOXICILLIN
Strength Number 25
Strength Unit mg/mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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