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"70518-0747-0" National Drug Code (NDC)
Nifedipine 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0747-0)
(REMEDYREPACK INC.)
NDC Code
70518-0747-0
Package Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-0747-0)
Product NDC
70518-0747
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Nifedipine
Non-Proprietary Name
Nifedipine
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20170925
Marketing Category Name
ANDA
Application Number
ANDA201071
Manufacturer
REMEDYREPACK INC.
Substance Name
NIFEDIPINE
Strength
30
Strength Unit
mg/1
Pharmacy Classes
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0747-0