Package 24979-010-12

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 24979-010-12
Digits Only 2497901012
Product NDC 24979-010
Description

300 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-010-12)

Marketing

Marketing Status
Marketed Since 2015-05-15
Brand nifedipine
Generic nifedipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "58c4c95e-4db0-47e2-afb9-36472e6fcefc", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013", "1812015"], "spl_set_id": ["160271a8-7922-2107-e054-00144ff88e88"], "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": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-010-12)", "package_ndc": "24979-010-12", "marketing_start_date": "20150515"}], "brand_name": "Nifedipine", "product_id": "24979-010_58c4c95e-4db0-47e2-afb9-36472e6fcefc", "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"}