Package 60687-875-01

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-875-01
Digits Only 6068787501
Product NDC 60687-875
Product ID 60687-875_3ed83eb8-0be6-13bd-e063-6394a90a831d
Description

100 BLISTER PACK in 1 CARTON (60687-875-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-875-11)

Marketing

Marketing Status
Marketed Since 2025-09-11
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": "3ed83eb8-0be6-13bd-e063-6394a90a831d", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["fc148d96-b868-4e45-b7d2-977faf431049"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-875-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-875-11)", "package_ndc": "60687-875-01", "marketing_start_date": "20250911"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "60687-875_3ed83eb8-0be6-13bd-e063-6394a90a831d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "60687-875", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20250911", "listing_expiration_date": "20261231"}