nifedipine

Generic: nifedipine

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nifedipine
Generic Name nifedipine
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

nifedipine 60 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-010
Product ID 24979-010_9987d031-2d2a-4a43-a185-f29e28617e31
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203126
Listing Expiration 2027-12-31
Marketing Start 2014-11-01

Pharmacologic Class

Established (EPC)
dihydropyridine calcium channel blocker [epc]
Mechanism of Action
calcium channel antagonists [moa]
Chemical Structure
dihydropyridines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24979010
Hyphenated Format 24979-010

Supplemental Identifiers

RxCUI
1812011 1812013 1812015
UNII
I9ZF7L6G2L
NUI
N0000000069 N0000175421 M0006414

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nifedipine (source: ndc)
Generic Name nifedipine (source: ndc)
Application Number ANDA203126 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 60 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-010-01)
source: ndc

Packages (1)

24979-010-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-010-01)

Ingredients (1)

nifedipine (60 mg/1)

Linked Drug Pages (2)

Nifedipine ndc-match (0.9) Nifedipine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9987d031-2d2a-4a43-a185-f29e28617e31", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013", "1812015"], "spl_set_id": ["3bf4282f-b063-4d35-8ef0-6f48b98e9deb"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-010-01)", "package_ndc": "24979-010-01", "marketing_start_date": "20141101"}], "brand_name": "Nifedipine", "product_id": "24979-010_9987d031-2d2a-4a43-a185-f29e28617e31", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "24979-010", "generic_name": "Nifedipine", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "60 mg/1"}], "application_number": "ANDA203126", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20271231"}