Package 68788-7676-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-7676-3
Digits Only 6878876763
Product NDC 68788-7676
Product ID 68788-7676_aea86f98-afde-49f8-85a1-5ce2d777cbc9
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-7676-3)

Marketing

Marketing Status
Marketed Since 2020-03-02
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydroxyzine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aea86f98-afde-49f8-85a1-5ce2d777cbc9", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["97f91413-b41a-4f5f-9978-429da0191e4e"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7676-3)", "package_ndc": "68788-7676-3", "marketing_start_date": "20200302"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "68788-7676_aea86f98-afde-49f8-85a1-5ce2d777cbc9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68788-7676", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088617", "marketing_category": "ANDA", "marketing_start_date": "20200302", "listing_expiration_date": "20261231"}