Package 68071-3017-6

{"route": ["ORAL"], "spl_id": "1d788e6f-633a-a344-e063-6294a90a90d1", "openfda": {"upc": ["0368071301731"], "unii": ["HDP7W44CIO"], "rxcui": ["995666"], "spl_set_id": ["64a508ae-768a-2fba-e053-2991aa0ac42d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-3017-1)", "package_ndc": "68071-3017-1", "marketing_start_date": "20180207"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3017-2)", "package_ndc": "68071-3017-2", "marketing_start_date": "20180207"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3017-3)", "package_ndc": "68071-3017-3", "marketing_start_date": "20180207"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3017-6)", "package_ndc": "68071-3017-6", "marketing_start_date": "20180207"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (68071-3017-7)", "package_ndc": "68071-3017-7", "marketing_start_date": "20180207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3017-9)", "package_ndc": "68071-3017-9", "marketing_start_date": "20180207"}], "brand_name": "MECLIZINE HYDROCHLORIDE", "product_id": "68071-3017_1d788e6f-633a-a344-e063-6294a90a90d1", "dosage_form": "TABLET", "pharm_class": ["Antiemetic [EPC]", "Emesis Suppression [PE]"], "product_ndc": "68071-3017", "generic_name": "Meclizine Hydrocloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MECLIZINE HYDROCHLORIDE", "active_ingredients": [{"name": "MECLIZINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040659", "marketing_category": "ANDA", "marketing_start_date": "20100604", "listing_expiration_date": "20261231"}