FDA.reportPublic FDA data

Nifedipine

Product NDC
68071-3364
11-digit product format
680713364
Labeler code
68071
Product ID
68071-3364_55f10368-1557-67f5-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nifedipine
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA077127
Marketing category
ANDA
Marketing start
2005-11-21
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
68071-3364-32020-05-13C16284748780-19d75b9d0-e3b0-f424-e053-dadaa90a57ce55f10368-1556-67f5-e054-00144ff88e88
68071-3364-62020-05-13C16284748780-19d75b9d0-e3b0-f424-e053-dadaa90a57ce55f10368-1556-67f5-e054-00144ff88e88
68071-3364-32020-01-31C16284748780-19d75b9d0-e3b0-f424-e053-dadaa90a57ce55f10368-1556-67f5-e054-00144ff88e88
68071-3364-62020-01-31C16284748780-19d75b9d0-e3b0-f424-e053-dadaa90a57ce55f10368-1556-67f5-e054-00144ff88e88