benadryl allergy ultratab

Generic: diphenhydramine hydrochloride

Labeler: jones healthcare group - packaging services, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name benadryl allergy ultratab
Generic Name diphenhydramine hydrochloride
Labeler jones healthcare group - packaging services, inc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
Jones Healthcare Group - Packaging Services, Inc

Identifiers & Regulatory

Product NDC 67414-226
Product ID 67414-226_0975230a-8706-cc07-e063-6294a90a3873
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-01-24

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 67414226
Hyphenated Format 67414-226

Supplemental Identifiers

RxCUI
1049630 1049632
UPC
0300450170606
UNII
TC2D6JAD40

Packaging Origin

Original Packager
true

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 ultratab (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
  • 2500 POUCH in 1 BOX (67414-226-00) / 2 TABLET, FILM COATED in 1 POUCH
  • 60 POUCH in 1 CARTON (67414-226-54) / 2 TABLET, FILM COATED in 1 POUCH
source: ndc

Packages (2)

67414-226-00 2500 POUCH in 1 BOX (67414-226-00) / 2 TABLET, FILM COATED in 1 POUCH 67414-226-54 60 POUCH in 1 CARTON (67414-226-54) / 2 TABLET, FILM COATED in 1 POUCH

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Benadryl Allergy Ultratab ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0975230a-8706-cc07-e063-6294a90a3873", "openfda": {"upc": ["0300450170606"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630", "1049632"], "spl_set_id": ["ec2070df-8a8a-4cd1-8830-62655433fb3b"], "manufacturer_name": ["Jones Healthcare Group - Packaging Services, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2500 POUCH in 1 BOX (67414-226-00)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67414-226-00", "marketing_start_date": "20180124"}, {"sample": false, "description": "60 POUCH in 1 CARTON (67414-226-54)  / 2 TABLET, FILM COATED in 1 POUCH", "package_ndc": "67414-226-54", "marketing_start_date": "20180124"}], "brand_name": "Benadryl Allergy Ultratab", "product_id": "67414-226_0975230a-8706-cc07-e063-6294a90a3873", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "67414-226", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "Jones Healthcare Group - Packaging Services, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Allergy Ultratab", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180124", "listing_expiration_date": "20261231"}