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
- 62135-010_45c62a1b-f162-d3cb-e063-6394a90a7dbf
- Product NDC
- 62135-010
- Form
- SOLUTION
- Composition / generic term
- Amantadine Hydrochloride
- Labeler
- Chartwell RX, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19930628
- Source listing expiry
- 20261231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 50 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (62135-010-47) · 62135-010-47
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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