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Amoxicillin - 67253-145-02 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 67253-145
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 875    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 67253-145
Labeler Name: DAVA International, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065344
Marketing Category: ANDA
Start Marketing Date: 20090715

Package Information of Amoxicillin

Package NDC: 67253-145-02
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (67253-145-02)

NDC Information of Amoxicillin

NDC Code 67253-145-02
Proprietary Name Amoxicillin
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (67253-145-02)
Product NDC 67253-145
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090715
Marketing Category Name ANDA
Labeler Name DAVA International, Inc.
Substance Name AMOXICILLIN
Strength Number 875
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Amoxicillin


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