Package 68382-690-77

Brand: nifedipine

Generic: nifedipine
NDC Package

Package Facts

Identity

Package NDC 68382-690-77
Digits Only 6838269077
Product NDC 68382-690
Description

10 BLISTER PACK in 1 CARTON (68382-690-77) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-08-18
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": "18f1ad21-11a1-4d2d-b5bc-a88ac8c02f45", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0368382688774", "0368382690777"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034", "198035", "198036"], "spl_set_id": ["1c857df2-9cce-40de-95c3-b1274ed1e1bc"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-01)", "package_ndc": "68382-690-01", "marketing_start_date": "20180818"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-10)", "package_ndc": "68382-690-10", "marketing_start_date": "20180818"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-16)", "package_ndc": "68382-690-16", "marketing_start_date": "20180818"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-690-77)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "68382-690-77", "marketing_start_date": "20180818"}, {"sample": false, "description": "300 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-690-95)", "package_ndc": "68382-690-95", "marketing_start_date": "20180818"}], "brand_name": "NIFEDIPINE", "product_id": "68382-690_18f1ad21-11a1-4d2d-b5bc-a88ac8c02f45", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68382-690", "generic_name": "NIFEDIPINE", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NIFEDIPINE", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "90 mg/1"}], "application_number": "ANDA210184", "marketing_category": "ANDA", "marketing_start_date": "20180818", "listing_expiration_date": "20261231"}