Package 83112-555-59

Brand: banophen

Generic: diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 83112-555-59
Digits Only 8311255559
Product NDC 83112-555
Product ID 83112-555_2cdbe7df-4c68-9b05-e063-6394a90a4699
Description

1 TABLET, FILM COATED in 1 PACKET (83112-555-59)

Marketing

Marketing Status
Marketed Since 2025-01-31
Brand banophen
Generic diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Banophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2cdbe7df-4c68-9b05-e063-6394a90a4699", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1092421"], "spl_set_id": ["2cdbe7df-4c67-9b05-e063-6394a90a4699"], "manufacturer_name": ["Health Department, Oklahoma State"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET, FILM COATED in 1 PACKET (83112-555-59)", "package_ndc": "83112-555-59", "marketing_start_date": "20250131"}], "brand_name": "Banophen", "product_id": "83112-555_2cdbe7df-4c68-9b05-e063-6394a90a4699", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83112-555", "generic_name": "Diphenhydramine HCl", "labeler_name": "Health Department, Oklahoma State", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Banophen", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20250131", "listing_expiration_date": "20261231"}