"53002-1804-0" National Drug Code (NDC)

Amlodipine And Benazepril Hydrochloride 100 CAPSULE in 1 BOTTLE (53002-1804-0)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-1804-0
Package Description100 CAPSULE in 1 BOTTLE (53002-1804-0)
Product NDC53002-1804
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine And Benazepril Hydrochloride
Non-Proprietary NameAmlodipine And Benazepril Hydrochloride
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20120905
Marketing Category NameANDA
Application NumberANDA202239
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength10; 40
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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