Package 70518-2679-0

{"route": ["ORAL"], "spl_id": "4a7dc836-cfa3-7c70-e063-6394a90a0df1", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011"], "spl_set_id": ["24e56333-5601-48fd-a263-f6be90983fb4"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2679-0)", "package_ndc": "70518-2679-0", "marketing_start_date": "20200408"}], "brand_name": "Nifedipine", "product_id": "70518-2679_4a7dc836-cfa3-7c70-e063-6394a90a0df1", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "70518-2679", "generic_name": "nifedipine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA210614", "marketing_category": "ANDA", "marketing_start_date": "20200408", "listing_expiration_date": "20271231"}