United States · FDA National Drug Code directory
Loperamide Hydrochloride
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
- 68016-123_0ea714a1-b048-bc87-e063-6294a90a28e7
- Product NDC
- 68016-123
- Form
- TABLET
- Composition / generic term
- Loperamide Hydrochloride
- Labeler
- Chain Drug Consortium, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19930201
- Source listing expiry
- 20261231
Source-listed ingredients
- LOPERAMIDE HYDROCHLORIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BLISTER PACK (68016-123-06) · 68016-123-06
- 18 TABLET in 1 BLISTER PACK (68016-123-18) · 68016-123-18
- 24 TABLET in 1 BLISTER PACK (68016-123-24) · 68016-123-24
- 96 TABLET in 1 BOTTLE (68016-123-97) · 68016-123-97
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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