Memantine Hydrochloride
- Product NDC
- 63629-7090
- 11-digit product format
- 636297090
- Labeler code
- 63629
- Product ID
- 63629-7090_46f4a10f-24c1-40bf-a0e4-91af3a09ac25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- memantine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA079225
- Marketing category
- ANDA
- Marketing start
- 2015-07-11
- Marketing end
- 0000-00-00
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 5 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7090-1 | 63629709001 | 30 TABLET in 1 BOTTLE (63629-7090-1) | 30 tablet | 2016-09-16 | 0000-00-00 | No | No | Current |