United States · FDA National Drug Code directory
Albendazole
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
- 72162-2359_875c188d-cbe0-410c-89c3-3e97a79c2d12
- Product NDC
- 72162-2359
- Form
- TABLET
- Composition / generic term
- Albendazole
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210224
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBENDAZOLE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET in 1 BOTTLE (72162-2359-2) · 72162-2359-2
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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