FDA.reportPublic FDA data

Nifedipine

Product NDC
68071-3315
11-digit product format
680713315
Labeler code
68071
Product ID
68071-3315_5163e676-12aa-0c09-e054-00144ff8d46c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nifedipine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA075269
Marketing category
ANDA
Marketing start
2000-12-04
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
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-3315-32020-05-13C16284748780-19d75b9d0-2944-f424-e053-dadaa90a57ce5163e676-12a9-0c09-e054-00144ff8d46c
68071-3315-62020-05-13C16284748780-19d75b9d0-2944-f424-e053-dadaa90a57ce5163e676-12a9-0c09-e054-00144ff8d46c
68071-3315-32020-01-31C16284748780-19d75b9d0-2944-f424-e053-dadaa90a57ce5163e676-12a9-0c09-e054-00144ff8d46c
68071-3315-62020-01-31C16284748780-19d75b9d0-2944-f424-e053-dadaa90a57ce5163e676-12a9-0c09-e054-00144ff8d46c