banophen

Generic: diphenhydramine hcl

Labeler: health department, oklahoma state
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name banophen
Generic Name diphenhydramine hcl
Labeler health department, oklahoma state
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
Health Department, Oklahoma State

Identifiers & Regulatory

Product NDC 83112-555
Product ID 83112-555_2cdbe7df-4c68-9b05-e063-6394a90a4699
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2025-01-31

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83112555
Hyphenated Format 83112-555

Supplemental Identifiers

RxCUI
1049630 1092421
UNII
TC2D6JAD40

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name banophen (source: ndc)
Generic Name diphenhydramine hcl (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1 TABLET, FILM COATED in 1 PACKET (83112-555-59)
source: ndc

Packages (1)

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

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Banophen ndc-match (0.9)

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"}