Amantadine Hydrochloride
- Product NDC
- 67046-1452
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amantadine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA209035
- Marketing category
- ANDA
- Substance
- AMANTADINE HYDROCHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 67046-1452-3 | 30 TABLET in 1 BLISTER PACK (67046-1452-3) | 2025-02-07 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Amantadine Hydrochloride Tablets | Coupler LLC | 2025-02-07 | HUMAN PRESCRIPTION DRUG LABEL | 1 |