Package 72789-486-01
Brand: nifedipine
Generic: nifedipinePackage Facts
Identity
Package NDC
72789-486-01
Digits Only
7278948601
Product NDC
72789-486
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-486-01)
Marketing
Marketing Status
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": "47bfdd27-82a6-09b7-e063-6294a90acc43", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0372789486017"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812015"], "spl_set_id": ["8e5e126a-7da6-4ceb-b72b-5c9dcc7d7769"], "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": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-486-01)", "package_ndc": "72789-486-01", "marketing_start_date": "20250212"}], "brand_name": "Nifedipine", "product_id": "72789-486_47bfdd27-82a6-09b7-e063-6294a90acc43", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72789-486", "generic_name": "Nifedipine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "90 mg/1"}], "application_number": "ANDA216067", "marketing_category": "ANDA", "marketing_start_date": "20220330", "listing_expiration_date": "20271231"}