Package 45865-675-20

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 45865-675-20
Digits Only 4586567520
Product NDC 45865-675
Product ID 45865-675_13170abe-54c9-4cb3-e063-6394a90a150b
Description

20 TABLET in 1 BOTTLE (45865-675-20)

Marketing

Marketing Status
Marketed Since 2023-03-21
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": "13170abe-54c9-4cb3-e063-6394a90a150b", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["13172e1e-2b62-8a67-e063-6394a90a3010"], "manufacturer_name": ["Medsource Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (45865-675-20)", "package_ndc": "45865-675-20", "marketing_start_date": "20230321"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "45865-675_13170abe-54c9-4cb3-e063-6394a90a150b", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "45865-675", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Medsource Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}