Package 68682-108-30

{"route": ["ORAL"], "spl_id": "68cca98c-658a-48b4-9630-478b62b1471e", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "upc": ["0368682108101"], "unii": ["I9ZF7L6G2L"], "rxcui": ["1812011", "1812013"], "spl_set_id": ["c7874606-c71e-424c-b881-38697988e0d0"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-10)", "package_ndc": "68682-108-10", "marketing_start_date": "20000927"}, {"sample": false, "description": "300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-108-30)", "package_ndc": "68682-108-30", "marketing_start_date": "20000927"}], "brand_name": "nifedipine", "product_id": "68682-108_68cca98c-658a-48b4-9630-478b62b1471e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "68682-108", "generic_name": "nifedipine", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "nifedipine", "active_ingredients": [{"name": "NIFEDIPINE", "strength": "30 mg/1"}], "application_number": "ANDA075289", "marketing_category": "ANDA", "marketing_start_date": "20000927", "listing_expiration_date": "20271231"}