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
- 42806-716_1497ce1d-a997-4828-a08d-3f93653a88d5
- Product NDC
- 42806-716
- Form
- CAPSULE
- Composition / generic term
- amantadine hydrochloride
- Labeler
- EPIC PHARMA LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210617
- Source listing expiry
- 20261231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 CAPSULE in 1 BOTTLE (42806-716-05) · 42806-716-05
- 10 CAPSULE in 1 BOTTLE (42806-716-11) · 42806-716-11
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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