Home > National Drug Code (NDC) > AMOXICILLIN

AMOXICILLIN - 43598-223-50 - (amoxicillin)

Alphabetical Index


Drug Information of AMOXICILLIN

Product NDC: 43598-223
Proprietary Name: AMOXICILLIN
Non Proprietary Name: amoxicillin
Active Ingredient(s): 200    mg/5mL & nbsp;   amoxicillin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of AMOXICILLIN

Product NDC: 43598-223
Labeler Name: Dr Reddys Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050760
Marketing Category: NDA
Start Marketing Date: 19990415

Package Information of AMOXICILLIN

Package NDC: 43598-223-50
Package Description: 50 mL in 1 BOTTLE (43598-223-50)

NDC Information of AMOXICILLIN

NDC Code 43598-223-50
Proprietary Name AMOXICILLIN
Package Description 50 mL in 1 BOTTLE (43598-223-50)
Product NDC 43598-223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19990415
Marketing Category Name NDA
Labeler Name Dr Reddys Laboratories Inc
Substance Name AMOXICILLIN
Strength Number 200
Strength Unit mg/5mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of AMOXICILLIN


General Information