Package 0904-7229-61

{"route": ["ORAL"], "spl_id": "4f81130b-db75-4292-9229-338914ccd6f3", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198032"], "spl_set_id": ["acb493a3-b8f2-41a9-8ab2-550d97c4592a"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7229-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7229-61", "marketing_start_date": "20220823"}], "brand_name": "Nifedipine", "product_id": "0904-7229_4f81130b-db75-4292-9229-338914ccd6f3", "dosage_form": "CAPSULE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "0904-7229", "generic_name": "Nifedipine", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "10 mg/1"}], "application_number": "ANDA202644", "marketing_category": "ANDA", "marketing_start_date": "20220823", "listing_expiration_date": "20261231"}