"70518-0600-0" National Drug Code (NDC)

Procardia 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0600-0)
(REMEDYREPACK INC.)

NDC Code70518-0600-0
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0600-0)
Product NDC70518-0600
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameProcardia
Proprietary Name SuffixXl
Non-Proprietary NameNifedipine
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170628
Marketing Category NameNDA
Application NumberNDA019684
ManufacturerREMEDYREPACK INC.
Substance NameNIFEDIPINE
Strength30
Strength Unitmg/1
Pharmacy ClassesCalcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]

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