Package 51655-080-53

{"route": ["ORAL"], "spl_id": "46ddd139-5487-4c55-e063-6294a90a6f64", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["c13455a3-3078-4fe1-e053-2a95a90adf8e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-080-20)", "package_ndc": "51655-080-20", "marketing_start_date": "20210420"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-080-25)", "package_ndc": "51655-080-25", "marketing_start_date": "20220415"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-080-52)", "package_ndc": "51655-080-52", "marketing_start_date": "20201210"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE, PLASTIC (51655-080-53)", "package_ndc": "51655-080-53", "marketing_start_date": "20230913"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "51655-080_46ddd139-5487-4c55-e063-6294a90a6f64", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "51655-080", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20271231"}