Memantine Hydrochloride
- Product NDC
- 63629-7333
- 11-digit product format
- 636297333
- Labeler code
- 63629
- Product ID
- 63629-7333_ecc37f57-3865-4b7a-a4e3-44331f4e2d55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Memantine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA206528
- Marketing category
- ANDA
- Marketing start
- 2015-08-27
- 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#