memantine hydrochloride
- Product NDC
- 16714-961
- 11-digit product format
- 167140961
- Labeler code
- 16714
- Product ID
- 16714-961_85c0c345-fa90-49b3-813c-51c53d9bd7a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- memantine hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA205905
- Marketing category
- ANDA
- Marketing start
- 2020-01-28
- Marketing end
- 0000-00-00
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 21 mg/1
- Pharmacologic classes
- NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-961-01 | 16714096101 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-961-01) | 2020-01-28 | 0000-00-00 | No | No | Current |