Package 80513-722-06

Brand: allergy relief

Generic: diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 80513-722-06
Digits Only 8051372206
Product NDC 80513-722
Product ID 80513-722_38ec4df3-7638-3adf-e063-6394a90a0cec
Description

600 TABLET in 1 BOTTLE (80513-722-06)

Marketing

Marketing Status
Discontinued 2027-12-31
Brand allergy relief
Generic diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Allergy Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38ec4df3-7638-3adf-e063-6394a90a0cec", "openfda": {"upc": ["0380513000927"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["20e164b8-4cbc-cf3f-e063-6394a90a9d0c"], "manufacturer_name": ["Advanced Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "600 TABLET in 1 BOTTLE (80513-722-06)", "package_ndc": "80513-722-06", "marketing_end_date": "20271231", "marketing_start_date": "20240801"}], "brand_name": "Allergy Relief", "product_id": "80513-722_38ec4df3-7638-3adf-e063-6394a90a0cec", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "80513-722", "generic_name": "Diphenhydramine HCl", "labeler_name": "Advanced Rx LLC", "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_end_date": "20271231", "marketing_start_date": "20240801"}