Package 60760-990-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-990-30
Digits Only 6076099030
Product NDC 60760-990
Product ID 60760-990_30b6f6a5-9c36-af93-e063-6294a90a0228
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-990-30)

Marketing

Marketing Status
Marketed Since 2025-03-19
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": "30b6f6a5-9c36-af93-e063-6294a90a0228", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["30b6f7b3-b620-961a-e063-6394a90a487b"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-990-30)", "package_ndc": "60760-990-30", "marketing_start_date": "20250319"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "60760-990_30b6f6a5-9c36-af93-e063-6294a90a0228", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "60760-990", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA217652", "marketing_category": "ANDA", "marketing_start_date": "20230822", "listing_expiration_date": "20261231"}