Nifedipine

Product NDC
50090-1843
11-digit product format
500901843
Labeler code
50090
Product ID
50090-1843_a75e27f8-72ca-4bac-9117-40ae4d0cca11
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nifedipine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA203126
Marketing category
ANDA
Marketing start
2014-11-01
Marketing end
0000-00-00
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-1843-0EA - Each50090-184384b114fc-0741-47d0-91f4-a8dc40683a8712021-09-07
50090-1843-2EA - Each50090-18435c8dbdb5-5efd-4440-9a21-a6c7c575234e12021-09-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-1843NIFEDIPINE TABLET, EXTENDED RELEASE [A-S MEDICATION SOLUTIONS]15Legacy NDC20230208_c09acb07-d9aa-4918-8ef1-b47b001d8a94.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-1843-05009018430030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1843-0) 2015-05-260000-00-00NoNoCurrent
50090-1843-150090184301100 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1843-1) 2015-05-260000-00-00NoNoCurrent
50090-1843-25009018430290 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1843-2) 2015-07-220000-00-00NoNoCurrent