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
- 42543-497_0b366abe-58d8-43b8-8d0e-3659aad1c4af
- Product NDC
- 42543-497
- Form
- TABLET
- Composition / generic term
- Amantadine Hydrochloride
- Labeler
- Strides Pharma Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170804
- Source listing expiry
- 20271231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (42543-497-01) · 42543-497-01
- 500 TABLET in 1 BOTTLE (42543-497-05) · 42543-497-05
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →