Memantine Hydrochloride
- Product NDC
- 63629-7732
- 11-digit product format
- 636297732
- Labeler code
- 63629
- Product ID
- 63629-7732_8b292d2c-3651-4316-9f49-d800816f7584
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- memantine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200022
- Marketing category
- ANDA
- Marketing start
- 2015-11-01
- 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
- 2020-12-31
- 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 |
|---|
| 63629-7732-1 | 63629773201 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7732-1) | 2018-06-08 | 0000-00-00 | No | No | Current |
| 63629-7732-2 | 63629773202 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-7732-2) | 2018-06-08 | 0000-00-00 | No | No | Current |