Nifedipine

Product NDC
71205-963
11-digit product format
712050963
Labeler code
71205
Product ID
71205-963_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
30 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
71205-963-0071205096300100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-00) 2020-06-09NoNoHistorical
71205-963-307120509633030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-30) 2020-10-06NoNoHistorical
71205-963-607120509636060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-60) 2020-10-06NoNoHistorical
71205-963-6471205096364240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-64) 2020-10-06NoNoHistorical
71205-963-6771205096367270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-67) 2020-10-06NoNoHistorical
71205-963-7271205096372120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-72) 2020-10-06NoNoHistorical
71205-963-7871205096378180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-78) 2020-10-06NoNoHistorical
71205-963-907120509639090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-90) 2020-10-06NoNoHistorical
71205-963-9671205096396300 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-963-96) 2020-06-09NoNoHistorical

Related DailyMed Labels

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