United States · FDA National Drug Code directory

Loperamide HCl

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
50844-735_cb21f56f-f513-4fa1-817c-0e5c3ce660c5
Product NDC
50844-735
Form
TABLET
Composition / generic term
Loperamide HCl
Labeler
L.N.K. International, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20050503
Source listing expiry
20261231

Source-listed ingredients

  • LOPERAMIDE HYDROCHLORIDE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 BLISTER PACK in 1 CARTON (50844-735-02) / 6 TABLET in 1 BLISTER PACK · 50844-735-02
  • 4 BLISTER PACK in 1 CARTON (50844-735-08) / 6 TABLET in 1 BLISTER PACK · 50844-735-08
  • 2 BLISTER PACK in 1 CARTON (50844-735-19) / 4 TABLET in 1 BLISTER PACK · 50844-735-19
  • 1 BLISTER PACK in 1 CARTON (50844-735-24) / 2 TABLET in 1 BLISTER PACK · 50844-735-24
  • 3 BLISTER PACK in 1 CARTON (50844-735-44) / 6 TABLET in 1 BLISTER PACK · 50844-735-44
  • 1 BLISTER PACK in 1 CARTON (50844-735-45) / 6 TABLET in 1 BLISTER PACK · 50844-735-45

Source and coverage

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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.

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