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"70518-0792-0" National Drug Code (NDC)

Nifedipine 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0792-0)
(REMEDYREPACK INC.)

NDC Code70518-0792-0
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0792-0)
Product NDC70518-0792
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNifedipine
Non-Proprietary NameNifedipine
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20171017
Marketing Category NameANDA
Application NumberANDA077127
ManufacturerREMEDYREPACK INC.
Substance NameNIFEDIPINE
Strength30
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/70518-0792-0





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