Package 72789-271-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-271-30
Digits Only 7278927130
Product NDC 72789-271
Product ID 72789-271_419e06f3-2fb6-ada1-e063-6294a90abe88
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-271-30)

Marketing

Marketing Status
Marketed Since 2022-09-07
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": "419e06f3-2fb6-ada1-e063-6294a90abe88", "openfda": {"upc": ["0372789271309"], "unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["7165a30c-09e4-4ca1-8548-bf71998ba12f"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-271-30)", "package_ndc": "72789-271-30", "marketing_start_date": "20220907"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72789-271_419e06f3-2fb6-ada1-e063-6294a90abe88", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72789-271", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "PD-Rx 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": "20130219", "listing_expiration_date": "20261231"}