United States · FDA National Drug Code directory
Amantadine
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
- 0116-4010_3479947d-22a8-67e8-e063-6294a90ae41c
- Product NDC
- 0116-4010
- Form
- SOLUTION
- Composition / generic term
- Amantadine
- Labeler
- Xttrium Laboratories, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241105
- Source listing expiry
- 20271231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 50 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (0116-4010-16) · 0116-4010-16
- 100 TRAY in 1 CASE (0116-4010-41) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4010-10) · 0116-4010-41
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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