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
- 0904-7042_e997ef48-cfa3-4aa8-bbea-be54c4c00f64
- Product NDC
- 0904-7042
- Form
- CAPSULE
- Composition / generic term
- Amantadine Hydrochloride
- Labeler
- Major Pharmaceuticals
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170612
- Source listing expiry
- 20271231
Source-listed ingredients
- AMANTADINE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 BLISTER PACK in 1 CARTON (0904-7042-06) / 1 CAPSULE in 1 BLISTER PACK · 0904-7042-06
- 500 CAPSULE in 1 BOTTLE (0904-7042-40) · 0904-7042-40
- 100 CAPSULE in 1 BOTTLE (0904-7042-59) · 0904-7042-59
- 100 BLISTER PACK in 1 CARTON (0904-7042-61) / 1 CAPSULE in 1 BLISTER PACK · 0904-7042-61
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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