Package 71610-841-60

{"route": ["ORAL"], "spl_id": "1b98b3b9-8ba8-309a-e063-6394a90aa64f", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["198034"], "spl_set_id": ["1b98b011-793c-ed92-e063-6294a90ac2bc"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-841-60)", "package_ndc": "71610-841-60", "marketing_start_date": "20240620"}], "brand_name": "Nifedipine", "product_id": "71610-841_1b98b3b9-8ba8-309a-e063-6394a90aa64f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "71610-841", "generic_name": "nifedipine", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA202987", "marketing_category": "ANDA", "marketing_start_date": "20170215", "listing_expiration_date": "20261231"}