"71821-002-01" National Drug Code (NDC)

NDC Code	71821-002-01
Package Description	250 TABLET, FILM COATED in 1 CONTAINER (71821-002-01)
Product NDC	71821-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ranitidine
Non-Proprietary Name	Ranitidine
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20190218
Marketing Category Name	ANDA
Application Number	ANDA211289
Manufacturer	VKT Pharma Private Limited
Substance Name	RANITIDINE HYDROCHLORIDE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]