Memantine Hydrochloride
- Product NDC
- 51407-285
- 11-digit product format
- 514070285
- Labeler code
- 51407
- Product ID
- 51407-285_9831193d-5a3c-664e-e053-2995a90a8888
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA207236
- Marketing category
- ANDA
- Marketing start
- 2016-11-10
- Marketing end
- 0000-00-00
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-285-60 | 51407028560 | 60 TABLET in 1 BOTTLE, PLASTIC (51407-285-60) | 60 tablet | 2019-10-30 | 0000-00-00 | No | No | Current |