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
- 50268-036_48c949ef-d92b-abba-e063-6394a90a2d2a
- Product NDC
- 50268-036
- Form
- SOLUTION
- Composition / generic term
- Amantadine
- Labeler
- AvPAK
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260119
- Source listing expiry
- 20271231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 50 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 40 TRAY in 1 CASE (50268-036-14) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (50268-036-11) · 50268-036-14
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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