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
- 72888-033_3982396f-63e5-ca93-e063-6394a90a75f2
- Product NDC
- 72888-033
- Form
- CAPSULE
- Composition / generic term
- Amantadine Hydrochloride
- Labeler
- Advagen Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200521
- Source listing expiry
- 20261231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 CAPSULE in 1 BOTTLE (72888-033-00) · 72888-033-00
- 100 CAPSULE in 1 BOTTLE (72888-033-01) · 72888-033-01
- 500 CAPSULE in 1 BOTTLE (72888-033-05) · 72888-033-05
- 30 CAPSULE in 1 BOTTLE (72888-033-30) · 72888-033-30
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 →