Memantine Hydrochloride
- Product NDC
- 16571-854
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- memantine
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA206032
- Marketing category
- ANDA
- Substance
- MEMANTINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 16571-854-03 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-854-03) | 2025-06-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Memantine Hydrochloride | Rising Pharma Holdings, Inc. | 2025-04-30 | HUMAN PRESCRIPTION DRUG LABEL | 3 |