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"57664-057-13" National Drug Code (NDC)

Amlodipine Besylate 500 TABLET in 1 BOTTLE (57664-057-13)
(Caraco Pharmaceutical Laboratories, Ltd.)

NDC Code57664-057-13
Package Description500 TABLET in 1 BOTTLE (57664-057-13)
Product NDC57664-057
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20121019
Marketing Category NameANDA
Application NumberANDA078552
ManufacturerCaraco Pharmaceutical Laboratories, Ltd.
Substance NameAMLODIPINE BESYLATE
Strength10
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/57664-057-13





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