"51991-896-33" National Drug Code (NDC)

NDC Code	51991-896-33
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (51991-896-33)
Product NDC	51991-896
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Entecavir
Non-Proprietary Name	Entecavir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20180316
End Marketing Date	20250131
Marketing Category Name	ANDA
Application Number	ANDA208721
Manufacturer	Breckenridge Pharmaceutical, Inc.
Substance Name	ENTECAVIR
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Analog [EXT], Nucleoside Reverse Transcriptase Inhibitors [MoA]