United States · FDA National Drug Code directory
Amantadine 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
- 0832-0111_45af44df-1a9b-32b6-e063-6394a90acdaf
- Product NDC
- 0832-0111
- Form
- TABLET
- Composition / generic term
- amantadine hydrochloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111215 / 20280229
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0832-0111-00) · 0832-0111-00
- 500 TABLET in 1 BOTTLE (0832-0111-50) · 0832-0111-50
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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