Package 55289-798-07

{"route": ["ORAL"], "spl_id": "419b65f7-5d45-aff4-e063-6294a90a2a36", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0355289798309"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011"], "spl_set_id": ["86c1bdae-c749-4ec3-90f6-7ebe8e76c461"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-798-07)", "package_ndc": "55289-798-07", "marketing_start_date": "20111021"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (55289-798-30)", "package_ndc": "55289-798-30", "marketing_start_date": "20111021"}], "brand_name": "Nifedipine", "product_id": "55289-798_419b65f7-5d45-aff4-e063-6294a90a2a36", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "55289-798", "generic_name": "Nifedipine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA077127", "marketing_category": "ANDA", "marketing_start_date": "20051121", "listing_expiration_date": "20261231"}