Package 72789-494-90

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 72789-494-90
Digits Only 7278949490
Product NDC 72789-494
Product ID 72789-494_30913851-9c5f-08ce-e063-6394a90aa7dd
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-494-90)

Marketing

Marketing Status
Marketed Since 2025-03-17
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": "30913851-9c5f-08ce-e063-6394a90aa7dd", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0372789494906"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812013"], "spl_set_id": ["75003769-7800-4bc7-b709-35b4caec2c2f"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-494-90)", "package_ndc": "72789-494-90", "marketing_start_date": "20250317"}], "brand_name": "Nifedipine", "product_id": "72789-494_30913851-9c5f-08ce-e063-6394a90aa7dd", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72789-494", "generic_name": "Nifedipine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}