Package 70518-1730-5

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1730-5
Digits Only 7051817305
Product NDC 70518-1730
Product ID 70518-1730_4962300f-0bce-8118-e063-6294a90af041
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-5)

Marketing

Marketing Status
Marketed Since 2025-06-18
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": "4962300f-0bce-8118-e063-6294a90af041", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["aa9523e0-c95d-4213-b213-96170d855536"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-5)", "package_ndc": "70518-1730-5", "marketing_start_date": "20250618"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-6)", "package_ndc": "70518-1730-6", "marketing_start_date": "20250618"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1730-7)", "package_ndc": "70518-1730-7", "marketing_start_date": "20251022"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "70518-1730_4962300f-0bce-8118-e063-6294a90af041", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "70518-1730", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040787", "marketing_category": "ANDA", "marketing_start_date": "20181213", "listing_expiration_date": "20271231"}