Package 31722-906-90

{"route": ["ORAL"], "spl_id": "540a17f8-b64d-41e1-a96b-d55bc8c48f3d", "openfda": {"upc": ["0331722906906"], "unii": ["3D867NP06J"], "rxcui": ["858625", "859033", "859040", "859044", "859048", "859052"], "spl_set_id": ["a7405a56-de1c-4875-b57f-210c991474ba"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-906-05)", "package_ndc": "31722-906-05", "marketing_start_date": "20150801"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (31722-906-10)", "package_ndc": "31722-906-10", "marketing_start_date": "20150801"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (31722-906-90)", "package_ndc": "31722-906-90", "marketing_start_date": "20150801"}], "brand_name": "PRAMIPEXOLE", "product_id": "31722-906_540a17f8-b64d-41e1-a96b-d55bc8c48f3d", "dosage_form": "TABLET", "pharm_class": ["Dopamine Agonists [MoA]", "Nonergot Dopamine Agonist [EPC]"], "product_ndc": "31722-906", "generic_name": "PRAMIPEXOLE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PRAMIPEXOLE", "active_ingredients": [{"name": "PRAMIPEXOLE DIHYDROCHLORIDE", "strength": ".125 mg/1"}], "application_number": "ANDA203855", "marketing_category": "ANDA", "marketing_start_date": "20150801", "listing_expiration_date": "20261231"}