benadryl

Generic: diphenhydramine hydrochloride

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

Drug Facts

Product Profile

Brand Name benadryl
Generic Name diphenhydramine hydrochloride
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 71205-521
Product ID 71205-521_e9c2a959-7772-43f4-a097-535c75b917bd
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2008-09-01

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 71205521
Hyphenated Format 71205-521

Supplemental Identifiers

RxCUI
1049630 1049632
UPC
0371205521066
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 benadryl (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 3 POUCH in 1 BAG (71205-521-06) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

71205-521-06 3 POUCH in 1 BAG (71205-521-06) / 2 TABLET, FILM COATED in 1 POUCH

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Benadryl ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e9c2a959-7772-43f4-a097-535c75b917bd", "openfda": {"upc": ["0371205521066"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["b1c849e5-8003-4fd3-811d-6a927523e353"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "3 POUCH in 1 BAG (71205-521-06)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "71205-521-06", "marketing_start_date": "20210101"}], "brand_name": "Benadryl", "product_id": "71205-521_e9c2a959-7772-43f4-a097-535c75b917bd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "71205-521", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20080901", "listing_expiration_date": "20261231"}