"64380-217-02" National Drug Code (NDC)

NDC Code	64380-217-02
Package Description	90 TABLET in 1 BOTTLE, PLASTIC (64380-217-02)
Product NDC	64380-217
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Valsartan
Non-Proprietary Name	Amlodipine And Valsartan
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20221024
Marketing Category Name	ANDA
Application Number	ANDA090011
Manufacturer	Strides Pharma Science Limited
Substance Name	AMLODIPINE; VALSARTAN
Strength	10; 320
Strength Unit	mg/1; mg/1
Pharmacy Classes	Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]