Package 70807-503-13

{"route": ["ORAL"], "spl_id": "3816123b-e06c-4abf-aead-2bed62b89c15", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0370807503135"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812015"], "spl_set_id": ["1df07edb-630d-4c70-a68c-bdbc607ce850"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Elite Pharmaceutical Solution, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-12)", "package_ndc": "70807-503-12", "marketing_start_date": "20211015"}, {"sample": false, "description": "300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70807-503-13)", "package_ndc": "70807-503-13", "marketing_start_date": "20211015"}], "brand_name": "nifedipine", "product_id": "70807-503_3816123b-e06c-4abf-aead-2bed62b89c15", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "70807-503", "generic_name": "nifedipine", "labeler_name": "Elite Pharmaceutical Solution, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "90 mg/1"}], "application_number": "ANDA212016", "marketing_category": "ANDA", "marketing_start_date": "20211015", "listing_expiration_date": "20271231"}