Package 68645-604-54

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 68645-604-54
Digits Only 6864560454
Product NDC 68645-604
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-604-54)

Marketing

Marketing Status
Marketed Since 2022-08-16
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": "4743ad3c-0518-566c-e063-6294a90aa06f", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0368645604541", "0368645603544"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013"], "spl_set_id": ["e65e1547-08ef-6682-e053-2a95a90a51b7"], "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 (68645-604-54)", "package_ndc": "68645-604-54", "marketing_start_date": "20220816"}], "brand_name": "Nifedipine", "product_id": "68645-604_4743ad3c-0518-566c-e063-6294a90aa06f", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68645-604", "generic_name": "Nifedipine", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "60 mg/1"}], "application_number": "ANDA077127", "marketing_category": "ANDA", "marketing_start_date": "20051121", "listing_expiration_date": "20261231"}