Memantine Hydrochloride
- Product NDC
- 64679-121
- 11-digit product format
- 646790121
- Labeler code
- 64679
- Product ID
- 64679-121_2377358b-8cd4-4446-9a83-83c05986fa74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA090073
- Marketing category
- ANDA
- Marketing start
- 2015-09-04
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#