Package 71335-2132-3
Brand: nifedipine
Generic: nifedipinePackage Facts
Identity
Package NDC
71335-2132-3
Digits Only
7133521323
Product NDC
71335-2132
Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-3)
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": "5cb5ba49-d959-4e98-8c12-efff26869287", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812015"], "spl_set_id": ["71a4e00b-8386-4da1-8515-a0e7e8db104d"], "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": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-1)", "package_ndc": "71335-2132-1", "marketing_start_date": "20220727"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-2)", "package_ndc": "71335-2132-2", "marketing_start_date": "20220727"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-3)", "package_ndc": "71335-2132-3", "marketing_start_date": "20220727"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-4)", "package_ndc": "71335-2132-4", "marketing_start_date": "20220727"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2132-5)", "package_ndc": "71335-2132-5", "marketing_start_date": "20220727"}], "brand_name": "Nifedipine", "product_id": "71335-2132_5cb5ba49-d959-4e98-8c12-efff26869287", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "71335-2132", "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": "ANDA210614", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}