Nifedipine

Product NDC
71205-964
11-digit product format
712050964
Labeler code
71205
Product ID
71205-964_ba67d6b0-f638-4264-9bd4-1557223abe83
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nifedipine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA203126
Marketing category
ANDA
Marketing start
2014-11-01
Substance
NIFEDIPINE
Active strength
60 mg/1
Pharmacologic classes
Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
I9ZF7L6G2LNIFEDIPINE21829-25-4NIFEDIPINE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71205-964-0071205096400100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-00) 2020-06-09NoNoHistorical
71205-964-307120509643030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-30) 2020-10-06NoNoHistorical
71205-964-607120509646060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-60) 2020-10-06NoNoHistorical
71205-964-6471205096464240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-64) 2020-10-06NoNoHistorical
71205-964-6771205096467270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-67) 2020-10-06NoNoHistorical
71205-964-7271205096472120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-72) 2020-10-06NoNoHistorical
71205-964-7871205096478180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-78) 2020-10-06NoNoHistorical
71205-964-907120509649090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-90) 2020-10-06NoNoHistorical
71205-964-9671205096496300 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-964-96) 2020-06-09NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NIFEdipine Extended-release Tablets, USPProficient Rx LP2022-03-01HUMAN PRESCRIPTION DRUG LABEL3