Package 68645-512-54

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 68645-512-54
Digits Only 6864551254
Product NDC 68645-512
Product ID 68645-512_4743abc2-f05c-01ce-e063-6394a90a9575
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-512-54)

Marketing

Marketing Status
Marketed Since 2005-11-21
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": "4743abc2-f05c-01ce-e063-6394a90a9575", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0368645512549", "0368645513546"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013"], "spl_set_id": ["09225078-e793-4578-bc34-2758a895720d"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-512-54)", "package_ndc": "68645-512-54", "marketing_start_date": "20051121"}], "brand_name": "Nifedipine", "product_id": "68645-512_4743abc2-f05c-01ce-e063-6394a90a9575", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68645-512", "generic_name": "Nifedipine", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA077127", "marketing_category": "ANDA", "marketing_start_date": "20051121", "listing_expiration_date": "20261231"}