"33342-016-12" National Drug Code (NDC)

NDC Code	33342-016-12
Package Description	100 TABLET in 1 CARTON (33342-016-12)
Product NDC	33342-016
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine
Non-Proprietary Name	Amlodipine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120413
Marketing Category Name	ANDA
Application Number	ANDA201380
Manufacturer	Macleods Pharmaceuticals Limited
Substance Name	AMLODIPINE BESYLATE
Strength	10
Strength Unit	mg/1