Package 43386-680-01

{"route": ["ORAL"], "spl_id": "21e7776e-65d0-45fb-a1b2-13f49055ad64", "openfda": {"upc": ["0343386680016"], "unii": ["F850569PQR", "A36BXO4PPX"], "rxcui": ["312289"], "spl_set_id": ["017ef042-40aa-44c9-baa8-037f06356845"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "100 TABLET in 1 BOTTLE (43386-680-01)", "package_ndc": "43386-680-01", "marketing_start_date": "20110511"}], "brand_name": "PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE", "product_id": "43386-680_21e7776e-65d0-45fb-a1b2-13f49055ad64", "dosage_form": "TABLET", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "43386-680", "dea_schedule": "CIV", "generic_name": "pentazocine hydrochloride and naloxone hydrochloride", "labeler_name": "Lupin Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PENTAZOCINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE", "active_ingredients": [{"name": "NALOXONE HYDROCHLORIDE", "strength": ".5 mg/1"}, {"name": "PENTAZOCINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA075735", "marketing_category": "ANDA", "marketing_start_date": "20110511", "listing_expiration_date": "20261231"}