Package 72162-2536-1
Brand: nifedipine
Generic: nifedipinePackage Facts
Identity
Package NDC
72162-2536-1
Digits Only
7216225361
Product NDC
72162-2536
Description
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2536-1)
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": "c113fe1f-2c51-4db8-8efe-1a295c79823b", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198036"], "spl_set_id": ["7dc5eec6-f32a-45e6-af24-830738cae471"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2536-1)", "package_ndc": "72162-2536-1", "marketing_start_date": "20250919"}], "brand_name": "Nifedipine", "product_id": "72162-2536_c113fe1f-2c51-4db8-8efe-1a295c79823b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72162-2536", "generic_name": "Nifedipine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "90 mg/1"}], "application_number": "ANDA213361", "marketing_category": "ANDA", "marketing_start_date": "20210719", "listing_expiration_date": "20261231"}