← FDA Drug Approvals (Drugs@FDA)
MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: MACLEODS PHARMS LTD · Approved 2025-07-15
Drug application
- FDA Application #
ANDA208672- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- MEMANTINE HYDROCHLORIDE AND DONEPEZIL HYDROCHLORIDE
- Generic name
- MEMANTINE AND DONEPEZIL
- Active ingredients
- DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- MACLEODS PHARMS LTD
- Manufacturer
- Macleods Pharmaceuticals Limited
- First approval
- 2025-07-15
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown