Memantine Hydrochloride
- Product NDC
- 63629-1985
- 11-digit product format
- 636291985
- Labeler code
- 63629
- Product ID
- 63629-1985_79f49375-8107-4816-bb4b-e09c9db13e8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205365
- Marketing category
- ANDA
- Marketing start
- 2020-05-19
- 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 |
|---|
| 63629-1985-1 | 63629198501 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-1985-1) | 2022-03-08 | 0000-00-00 | No | No | Current |