Memantine Hydrochloride
- Product NDC
- 42934-300
- 11-digit product format
- 429340300
- Labeler code
- 42934
- Product ID
- 42934-300_aecb951d-a5af-1a10-e053-2a95a90ab426
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride Oral
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Medley Pharmaceuticals Limited
- Application
- ANDA210319
- Marketing category
- ANDA
- Marketing start
- 2017-04-22
- Marketing end
- 0000-00-00
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 2 mg/mL
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42934-300-31 | 42934030031 | 360 mL in 1 BOTTLE (42934-300-31) | 360 ml | 2017-04-22 | 0000-00-00 | No | No | Current |