Package 68071-3450-4

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3450-4
Digits Only 6807134504
Product NDC 68071-3450
Product ID 68071-3450_2d674f1c-812e-5feb-e063-6294a90a2aeb
Description

4 TABLET in 1 BOTTLE (68071-3450-4)

Marketing

Marketing Status
Marketed Since 2023-07-06
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": "2d674f1c-812e-5feb-e063-6294a90a2aeb", "openfda": {"upc": ["0368071345049"], "unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["ffd33207-3f35-3486-e053-6394a90ac0ae"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (68071-3450-4)", "package_ndc": "68071-3450-4", "marketing_start_date": "20230706"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "68071-3450_2d674f1c-812e-5feb-e063-6294a90a2aeb", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68071-3450", "generic_name": "HydrOXYzine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrOXYzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040840", "marketing_category": "ANDA", "marketing_start_date": "20091111", "listing_expiration_date": "20261231"}