Memantine Hydrochloride
- Product NDC
- 63629-2222
- 11-digit product format
- 636292222
- Labeler code
- 63629
- Product ID
- 63629-2222_ccf953c6-7bb0-4358-aa42-11b37abf2a4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205784
- Marketing category
- ANDA
- Marketing start
- 2018-02-20
- Marketing end
- 0000-00-00
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 14 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 |
|---|
| 63629-2222-1 | 63629222201 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63629-2222-1) | 2021-03-22 | 0000-00-00 | No | No | Current |