United States · FDA National Drug Code directory

MEDIQUE Diamode

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
71205-316_0f3c6538-799e-4147-9407-df86b8668c00
Product NDC
71205-316
Form
TABLET
Composition / generic term
Loperamide Hydrochloride
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20081230
Source listing expiry
20261231

Source-listed ingredients

  • LOPERAMIDE HYDROCHLORIDE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TABLET in 1 PACKET (71205-316-01) · 71205-316-01
  • 6 TABLET in 1 PACKET (71205-316-06) · 71205-316-06

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.

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