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AMOXICILLIN - 43598-219-14 - (amoxicillin)

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Drug Information of AMOXICILLIN

Product NDC: 43598-219
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: 43598-219
Labeler Name: Dr Reddys Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050754
Marketing Category: NDA
Start Marketing Date: 19780710

Package Information of AMOXICILLIN

Package NDC: 43598-219-14
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (43598-219-14)

NDC Information of AMOXICILLIN

NDC Code 43598-219-14
Proprietary Name AMOXICILLIN
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (43598-219-14)
Product NDC 43598-219
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19780710
Marketing Category Name NDA
Labeler Name Dr Reddys Laboratories Inc
Substance Name AMOXICILLIN
Strength Number 875
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of AMOXICILLIN


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