allergy relief

Generic: diphenhydramine hcl

Labeler: l.n.k. international, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name diphenhydramine hcl
Labeler l.n.k. international, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
L.N.K. International, Inc.

Identifiers & Regulatory

Product NDC 50844-329
Product ID 50844-329_28490745-78ca-43e9-906c-b6d44fcdb4bb
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 50844329
Hyphenated Format 50844-329

Supplemental Identifiers

RxCUI
1049630
UPC
0050844329072
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 allergy relief (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
  • 1 BLISTER PACK in 1 CARTON (50844-329-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (50844-329-07) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (50844-329-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-12)
  • 4 BLISTER PACK in 1 CARTON (50844-329-22) / 12 TABLET, FILM COATED in 1 BLISTER PACK
  • 365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-51)
  • 600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-78)
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-329-82) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (8)

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "28490745-78ca-43e9-906c-b6d44fcdb4bb", "openfda": {"upc": ["0050844329072"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["db264d2f-bf81-4da2-8595-2bfa1e4ba2f1"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50844-329-02)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-329-02", "marketing_start_date": "19900302"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (50844-329-07)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-329-07", "marketing_start_date": "19900302"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (50844-329-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-329-08", "marketing_start_date": "19900302"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-12)", "package_ndc": "50844-329-12", "marketing_start_date": "19900302"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (50844-329-22)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50844-329-22", "marketing_start_date": "19900302"}, {"sample": false, "description": "365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-51)", "package_ndc": "50844-329-51", "marketing_start_date": "19900302"}, {"sample": false, "description": "600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-78)", "package_ndc": "50844-329-78", "marketing_start_date": "19900302"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-329-82)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-329-82", "marketing_start_date": "19900302"}], "brand_name": "Allergy Relief", "product_id": "50844-329_28490745-78ca-43e9-906c-b6d44fcdb4bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "50844-329", "generic_name": "Diphenhydramine HCl", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "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"}