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
- 70771-1769_b43ff8ed-7175-4a7a-8e42-5c66324b495c
- Product NDC
- 70771-1769
- Form
- CAPSULE
- Composition / generic term
- Loperamide hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230625
- Source listing expiry
- 20261231
Source-listed ingredients
- LOPERAMIDE HYDROCHLORIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (70771-1769-1) · 70771-1769-1
- 10 BLISTER PACK in 1 CARTON (70771-1769-4) / 10 CAPSULE in 1 BLISTER PACK (70771-1769-2) · 70771-1769-4
- 500 CAPSULE in 1 BOTTLE (70771-1769-5) · 70771-1769-5
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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