benadryl allergy

Generic: diphenhydramine hydrochloride

Labeler: r j general corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benadryl allergy
Generic Name diphenhydramine hydrochloride
Labeler r j general corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
R J General Corporation

Identifiers & Regulatory

Product NDC 70264-024
Product ID 70264-024_43c8a290-73a2-52bb-e063-6294a90af527
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-03-01

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 70264024
Hyphenated Format 70264-024

Supplemental Identifiers

RxCUI
1049630 1049632
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 allergy (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
  • 30 POUCH in 1 CARTON (70264-024-01) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (1)

70264-024-01 30 POUCH in 1 CARTON (70264-024-01) / 2 TABLET, FILM COATED in 1 POUCH

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Benadryl Allergy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43c8a290-73a2-52bb-e063-6294a90af527", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["c46c01c0-29f4-400c-bef5-14b3eb944c51"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (70264-024-01)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "70264-024-01", "marketing_start_date": "20221226"}], "brand_name": "Benadryl Allergy", "product_id": "70264-024_43c8a290-73a2-52bb-e063-6294a90af527", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "70264-024", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Allergy", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220301", "listing_expiration_date": "20261231"}