Package 51655-593-26

{"route": ["ORAL"], "spl_id": "494efb4b-e4f9-e991-e063-6294a90a7af8", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011"], "spl_set_id": ["f32c0fc9-b4ad-6a1f-e053-2995a90acf61"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-593-26)", "package_ndc": "51655-593-26", "marketing_start_date": "20230103"}], "brand_name": "Nifedipine", "product_id": "51655-593_494efb4b-e4f9-e991-e063-6294a90a7af8", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "51655-593", "generic_name": "nifedipine", "labeler_name": "Northwind Health Company, LLC", "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": "20230103", "listing_expiration_date": "20271231"}