banophen

Generic: diphenhydramine hcl

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name banophen
Generic Name diphenhydramine hcl
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-611
Product ID 71205-611_449c7ca6-7fd4-4728-b330-2a3e261c6693
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 1990-03-02

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 71205611
Hyphenated Format 71205-611

Supplemental Identifiers

RxCUI
1049630 1092421
UPC
0371205611200
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)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-90)
source: ndc

Packages (4)

71205-611-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-20) 71205-611-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-30) 71205-611-60 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-60) 71205-611-90 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-90)

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": "449c7ca6-7fd4-4728-b330-2a3e261c6693", "openfda": {"upc": ["0371205611200"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1092421"], "spl_set_id": ["62934d0f-b23d-4c03-9d60-a7bad41f9b42"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-20)", "package_ndc": "71205-611-20", "marketing_start_date": "20211011"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-30)", "package_ndc": "71205-611-30", "marketing_start_date": "20211011"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-60)", "package_ndc": "71205-611-60", "marketing_start_date": "20211011"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-611-90)", "package_ndc": "71205-611-90", "marketing_start_date": "20211011"}], "brand_name": "Banophen", "product_id": "71205-611_449c7ca6-7fd4-4728-b330-2a3e261c6693", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-611", "generic_name": "Diphenhydramine HCl", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Banophen", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "19900302", "listing_expiration_date": "20261231"}