"49930-002-02" National Drug Code (NDC)

NDC Code	49930-002-02
Package Description	1000 TABLET, FILM COATED in 1 BOTTLE (49930-002-02)
Product NDC	49930-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Metoprolol Tartrate
Non-Proprietary Name	Metoprolol Tartrate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20141117
Marketing Category Name	ANDA
Application Number	ANDA200981
Manufacturer	Rubicon Research Private Limited
Substance Name	METOPROLOL TARTRATE
Strength	50
Strength Unit	mg/1
Pharmacy Classes	Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]