Package 68788-7642-3

{"route": ["ORAL"], "spl_id": "902d31db-8e45-4221-9308-2f02ea622a4c", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011"], "spl_set_id": ["4ee466dc-5a4e-4c77-8e94-8b510cafd61b"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-1)", "package_ndc": "68788-7642-1", "marketing_start_date": "20200228"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-3)", "package_ndc": "68788-7642-3", "marketing_start_date": "20200228"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-6)", "package_ndc": "68788-7642-6", "marketing_start_date": "20200228"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7642-9)", "package_ndc": "68788-7642-9", "marketing_start_date": "20200228"}], "brand_name": "Nifedipine", "product_id": "68788-7642_902d31db-8e45-4221-9308-2f02ea622a4c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68788-7642", "generic_name": "nifedipine", "labeler_name": "Preferred Pharmaceuticals, 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": "20200228", "listing_expiration_date": "20261231"}