Memantine Hydrochloride
- Product NDC
- 16571-854
- 11-digit product format
- 165710854
- Labeler code
- 16571
- Product ID
- 16571-854_4ece2bda-d26f-494f-93df-bc53c494caf9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- memantine
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Rising Pharma Holdings, Inc.
- Application
- ANDA206032
- Marketing category
- ANDA
- Marketing start
- 2025-06-01
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 21 mg/1
- Pharmacologic classes
- N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Memantine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MEMANTINE HYDROCHLORIDE | 21 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JY0WD0UA60 |
| Rxcui | 996594, 996603, 996609, 996615 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 16571-854-03 | Memantine Hydrochloride | 30 in 1 BOTTLE, PLASTIC | CAPSULE, EXTENDED RELEASE | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 16571-854 | MEMANTINE HYDROCHLORIDE (MEMANTINE) CAPSULE, EXTENDED RELEASE [RISING PHARMA HOLDINGS, INC.] | 2 | Current NDC, 1 package rows | 20250424_a282fbed-8304-458e-a0e9-5eaccc95339b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 16571-854-03 | 16571085403 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-854-03) | 2025-06-01 | No | No | Current |