diphenhydramine hydrochloride

Generic: diphenhydramine hydrochloride

Labeler: advance pharmaceutical inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name diphenhydramine hydrochloride
Generic Name diphenhydramine hydrochloride
Labeler advance pharmaceutical inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
Advance Pharmaceutical Inc.

Identifiers & Regulatory

Product NDC 17714-135
Product ID 17714-135_60f4322f-5c99-096a-e053-2a91aa0a64eb
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part341
Listing Expiration 2026-12-31
Marketing Start 2006-09-26

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 17714135
Hyphenated Format 17714-135

Supplemental Identifiers

RxCUI
1049630
UPC
0017714135010
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 diphenhydramine hydrochloride (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number part341 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (17714-135-01)
source: ndc

Packages (1)

17714-135-01 100 TABLET in 1 BOTTLE (17714-135-01)

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Diphenhydramine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "60f4322f-5c99-096a-e053-2a91aa0a64eb", "openfda": {"upc": ["0017714135010"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["c80f9a4c-1055-45d2-8fde-5b57fad3c82a"], "manufacturer_name": ["Advance Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (17714-135-01)", "package_ndc": "17714-135-01", "marketing_start_date": "20060926"}], "brand_name": "Diphenhydramine Hydrochloride", "product_id": "17714-135_60f4322f-5c99-096a-e053-2a91aa0a64eb", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "17714-135", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Advance Pharmaceutical Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20060926", "listing_expiration_date": "20261231"}