Package 70771-1365-5
Brand: nifedipine
Generic: nifedipinePackage Facts
Identity
Package NDC
70771-1365-5
Digits Only
7077113655
Product NDC
70771-1365
Description
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-5)
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": "b4ac4791-5cb1-4199-b56f-4171fd16fc33", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034", "198035", "198036"], "spl_set_id": ["925e2ea9-f51a-4b89-ab5d-ce590b6c4d85"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-0)", "package_ndc": "70771-1365-0", "marketing_start_date": "20180818"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-1)", "package_ndc": "70771-1365-1", "marketing_start_date": "20180818"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1365-4) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "70771-1365-4", "marketing_start_date": "20180818"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-5)", "package_ndc": "70771-1365-5", "marketing_start_date": "20180818"}, {"sample": false, "description": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-7)", "package_ndc": "70771-1365-7", "marketing_start_date": "20180818"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1365-9)", "package_ndc": "70771-1365-9", "marketing_start_date": "20180818"}], "brand_name": "NIFEDIPINE", "product_id": "70771-1365_b4ac4791-5cb1-4199-b56f-4171fd16fc33", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "70771-1365", "generic_name": "NIFEDIPINE", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NIFEDIPINE", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA210184", "marketing_category": "ANDA", "marketing_start_date": "20180818", "listing_expiration_date": "20261231"}