Package 0363-9024-60

Brand: allergy relief

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0363-9024-60
Digits Only 0363902460
Product NDC 0363-9024
Description

600 TABLET, FILM COATED in 1 BOTTLE (0363-9024-60)

Marketing

Marketing Status
Marketed Since 2022-06-14
Brand allergy relief
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a7f4d44-e9d0-d422-e063-6394a90a8e80", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["2b7aa3f5-3bc9-471f-8ff7-3c52719f0acb"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET, FILM COATED in 1 BOTTLE (0363-9024-60)", "package_ndc": "0363-9024-60", "marketing_start_date": "20220614"}], "brand_name": "Allergy Relief", "product_id": "0363-9024_2a7f4d44-e9d0-d422-e063-6394a90a8e80", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0363-9024", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220614", "listing_expiration_date": "20261231"}