Memantine Hydrochloride
- Product NDC
- 51407-054
- 11-digit product format
- 514070054
- Labeler code
- 51407
- Product ID
- 51407-054_e64f4296-583c-03d8-e053-2995a90a1835
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA205784
- Marketing category
- ANDA
- Marketing start
- 2017-06-09
- Marketing end
- 0000-00-00
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 7 mg/1
- Pharmacologic classes
- N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 51407-054-30 | 51407005430 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51407-054-30) | 2018-02-27 | 0000-00-00 | No | No | Current |