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
- 39328-530_f923b293-f2ac-4116-a122-9524fe748aca
- Product NDC
- 39328-530
- Form
- SOLUTION
- Composition / generic term
- amantadine hydrochloride
- Labeler
- Patrin Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230811
- 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, PLASTIC (39328-530-16) · 39328-530-16
- 10 TRAY in 1 CASE (39328-530-99) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (39328-530-10) · 39328-530-99
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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