Package 31722-502-10

{"route": ["ORAL"], "spl_id": "ee32d5bd-38fb-4a93-e053-2a95a90a0464", "openfda": {"upc": ["0331722502016", "0331722501019", "0331722500012"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["f7e527fe-2f67-45ad-a3ec-146ead819514"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-502-01)", "package_ndc": "31722-502-01", "marketing_start_date": "20080529"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-502-05)", "package_ndc": "31722-502-05", "marketing_start_date": "20080529"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-502-10)", "package_ndc": "31722-502-10", "marketing_start_date": "20080529"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "31722-502_ee32d5bd-38fb-4a93-e053-2a95a90a0464", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "31722-502", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040805", "marketing_category": "ANDA", "marketing_start_date": "20080529", "listing_expiration_date": "20261231"}