Nifedipine

Product NDC
71205-965
11-digit product format
712050965
Labeler code
71205
Product ID
71205-965_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
90 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
71205-965-0071205096500100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-00) 2020-06-09NoNoHistorical
71205-965-307120509653030 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-30) 2020-10-06NoNoHistorical
71205-965-607120509656060 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-60) 2020-10-06NoNoHistorical
71205-965-6471205096564240 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-64) 2020-10-06NoNoHistorical
71205-965-6771205096567270 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-67) 2020-10-06NoNoHistorical
71205-965-7271205096572120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-72) 2020-10-06NoNoHistorical
71205-965-7871205096578180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-78) 2020-10-06NoNoHistorical
71205-965-907120509659090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-90) 2020-10-06NoNoHistorical
71205-965-9671205096596300 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-965-96) 2020-06-09NoNoHistorical

Related DailyMed Labels

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