Package 43063-627-28

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-627-28
Digits Only 4306362728
Product NDC 43063-627
Product ID 43063-627_4139c958-3716-6915-e063-6394a90a690f
Description

28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-627-28)

Marketing

Marketing Status
Marketed Since 2015-10-28
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": "4139c958-3716-6915-e063-6394a90a690f", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["cc6a12ed-411b-4b0c-8108-58ef7db8da55"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-627-28)", "package_ndc": "43063-627-28", "marketing_start_date": "20151028"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "43063-627_4139c958-3716-6915-e063-6394a90a690f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "43063-627", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040786", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}