Package 72162-1277-9
Brand: nifedipine
Generic: nifedipinePackage Facts
Identity
Package NDC
72162-1277-9
Digits Only
7216212779
Product NDC
72162-1277
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1277-9)
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": "d713ebf4-6b8a-44ed-9fc2-0e1b34f6bb5f", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011"], "spl_set_id": ["4c4f8a8e-3995-4d2e-85d4-b6a45f5fac3e"], "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 (72162-1277-1)", "package_ndc": "72162-1277-1", "marketing_start_date": "20230508"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1277-3)", "package_ndc": "72162-1277-3", "marketing_start_date": "20230508"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1277-9)", "package_ndc": "72162-1277-9", "marketing_start_date": "20230508"}], "brand_name": "Nifedipine", "product_id": "72162-1277_d713ebf4-6b8a-44ed-9fc2-0e1b34f6bb5f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "72162-1277", "generic_name": "Nifedipine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA203126", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}