United States · FDA National Drug Code directory

Allergy Relief

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
50844-329_c32f9c98-7532-4e52-b09d-45534043e8ea
Product NDC
50844-329
Form
TABLET, FILM COATED
Composition / generic term
Diphenhydramine HCl
Labeler
L.N.K. International, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
19900302
Source listing expiry
20271231

Source-listed ingredients

  • DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CARTON (50844-329-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK · 50844-329-02
  • 3 BLISTER PACK in 1 CARTON (50844-329-07) / 12 TABLET, FILM COATED in 1 BLISTER PACK · 50844-329-07
  • 2 BLISTER PACK in 1 CARTON (50844-329-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK · 50844-329-08
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-12) · 50844-329-12
  • 4 BLISTER PACK in 1 CARTON (50844-329-22) / 12 TABLET, FILM COATED in 1 BLISTER PACK · 50844-329-22
  • 365 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-51) · 50844-329-51
  • 600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-329-78) · 50844-329-78
  • 1 BOTTLE, PLASTIC in 1 CARTON (50844-329-82) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 50844-329-82

Source and coverage

Open FDA National Drug Code directory →

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →