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"53002-2249-3" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BOTTLE (53002-2249-3)
(RPK Pharmaceuticals, Inc.)

NDC Code53002-2249-3
Package Description30 TABLET in 1 BOTTLE (53002-2249-3)
Product NDC53002-2249
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20140303
Marketing Category NameANDA
Application NumberANDA203245
ManufacturerRPK Pharmaceuticals, Inc.
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53002-2249-3





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