Package 24979-011-01

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 24979-011-01
Digits Only 2497901101
Product NDC 24979-011
Product ID 24979-011_9987d031-2d2a-4a43-a185-f29e28617e31
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-011-01)

Marketing

Marketing Status
Marketed Since 2014-11-01
Brand nifedipine
Generic nifedipine
Sample Package No

Linked Drug Pages (1)

Nifedipine ndc-match (0.95)

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, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-011-01)", "package_ndc": "24979-011-01", "marketing_start_date": "20141101"}], "brand_name": "Nifedipine", "product_id": "24979-011_9987d031-2d2a-4a43-a185-f29e28617e31", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "24979-011", "generic_name": "Nifedipine", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA203126", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20271231"}