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"67877-199-38" National Drug Code (NDC)

Amlodipine Besylate 10 BLISTER PACK in 1 CARTON (67877-199-38) / 10 TABLET in 1 BLISTER PACK
(Ascend Laboratories, LLC)

NDC Code67877-199-38
Package Description10 BLISTER PACK in 1 CARTON (67877-199-38) / 10 TABLET in 1 BLISTER PACK
Product NDC67877-199
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAmlodipine Besylate
Non-Proprietary NameAmlodipine Besylate
Dosage FormTABLET
UsageORAL
Start Marketing Date20101020
Marketing Category NameANDA
Application NumberANDA078925
ManufacturerAscend Laboratories, LLC
Substance NameAMLODIPINE BESYLATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67877-199-38





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