Package 68788-7854-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-7854-3
Digits Only 6878878543
Product NDC 68788-7854
Description

30 TABLET in 1 BOTTLE (68788-7854-3)

Marketing

Marketing Status
Marketed Since 2021-01-29
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d2ffcd08-7f0a-4113-aef3-050e49e7d4ee", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["63fdf791-1a58-45ba-8ef2-15b80bb24f23"], "manufacturer_name": ["Preferred Pharmaceuticals Incl"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7854-3)", "package_ndc": "68788-7854-3", "marketing_start_date": "20210129"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7854-6)", "package_ndc": "68788-7854-6", "marketing_start_date": "20210129"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7854-9)", "package_ndc": "68788-7854-9", "marketing_start_date": "20210129"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "68788-7854_d2ffcd08-7f0a-4113-aef3-050e49e7d4ee", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68788-7854", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Preferred Pharmaceuticals Incl", "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": "20210129", "listing_expiration_date": "20261231"}