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"52125-970-02" National Drug Code (NDC)

Nifedipine 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-970-02)
(REMEDYREPACK INC.)

NDC Code52125-970-02
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (52125-970-02)
Product NDC52125-970
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNifedipine
Non-Proprietary NameNifedipine
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20140616
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA019684
ManufacturerREMEDYREPACK INC.
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/52125-970-02





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