Package 60760-971-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-971-30
Digits Only 6076097130
Product NDC 60760-971
Product ID 60760-971_1767b4b1-074c-3373-e063-6294a90aca05
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-971-30)

Marketing

Marketing Status
Marketed Since 2024-04-09
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": "1767b4b1-074c-3373-e063-6294a90aca05", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["1767a886-ec92-39fb-e063-6294a90a1249"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-971-30)", "package_ndc": "60760-971-30", "marketing_start_date": "20240409"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "60760-971_1767b4b1-074c-3373-e063-6294a90aca05", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "60760-971", "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": "ANDA088618", "marketing_category": "ANDA", "marketing_start_date": "20121009", "listing_expiration_date": "20261231"}