Package 68788-7934-6

{"route": ["ORAL"], "spl_id": "4b5a138a-e5aa-4f49-a838-0e77480d4534", "openfda": {"unii": ["SOD6A38AGA"], "rxcui": ["855172"], "spl_set_id": ["8f308352-5854-409e-8bf7-bc9958cc3c5e"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7934-1)", "package_ndc": "68788-7934-1", "marketing_start_date": "20210615"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7934-3)", "package_ndc": "68788-7934-3", "marketing_start_date": "20210615"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7934-6)", "package_ndc": "68788-7934-6", "marketing_start_date": "20210615"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7934-9)", "package_ndc": "68788-7934-9", "marketing_start_date": "20210615"}], "brand_name": "levocetirizine dihydrochloride", "product_id": "68788-7934_4b5a138a-e5aa-4f49-a838-0e77480d4534", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "68788-7934", "generic_name": "levocetirizine dihydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levocetirizine dihydrochloride", "active_ingredients": [{"name": "LEVOCETIRIZINE DIHYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203646", "marketing_category": "ANDA", "marketing_start_date": "20210615", "listing_expiration_date": "20261231"}