Memantine Hydrochloride
- Product NDC
- 42292-006
- 11-digit product format
- 422920006
- Labeler code
- 42292
- Product ID
- 42292-006_7cef9597-5846-339f-e053-2991aa0a1efb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- memantine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA079225
- Marketing category
- ANDA
- Marketing start
- 2015-07-31
- Marketing end
- 2019-10-31
- Substance
- MEMANTINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record