Package 17856-0507-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17856-0507-1
Digits Only 1785605071
Product NDC 17856-0507
Product ID 17856-0507_34f4870b-c857-c0d9-e063-6294a90a011a
Description

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0507-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0507-2)

Marketing

Marketing Status
Marketed Since 2024-05-08
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": "34f4870b-c857-c0d9-e063-6294a90a011a", "openfda": {"unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["a2fbc502-6ca3-4304-9069-b7249c9d9489"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0507-1)  / 5 mL in 1 CUP, UNIT-DOSE (17856-0507-2)", "package_ndc": "17856-0507-1", "marketing_start_date": "20240508"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "17856-0507_34f4870b-c857-c0d9-e063-6294a90a011a", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "17856-0507", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA201674", "marketing_category": "ANDA", "marketing_start_date": "20130821", "listing_expiration_date": "20261231"}