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"63739-805-43" National Drug Code (NDC)

Nifedipine 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63739-805-43)
(McKesson Corporation)

NDC Code63739-805-43
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63739-805-43)
Product NDC63739-805
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNifedipine
Non-Proprietary NameNifedipine
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20110701
Marketing Category NameANDA
Application NumberANDA077899
ManufacturerMcKesson Corporation
Substance NameNIFEDIPINE
Strength30
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63739-805-43





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