"53808-1029-1" National Drug Code (NDC)

Amlodipine Besylate 30 TABLET in 1 BLISTER PACK (53808-1029-1)
(State of Florida DOH Central Pharmacy)

NDC Code53808-1029-1
Package Description30 TABLET in 1 BLISTER PACK (53808-1029-1)
Product NDC53808-1029
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20141101
Marketing Category NameANDA
Application NumberANDA078414
ManufacturerState of Florida DOH Central Pharmacy
Substance NameAMLODIPINE BESYLATE
Strength5
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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