Macleods Pharmaceuticals Limited
District Solan, India · makes it, tests it, packages it and labels it
Problems found, fixed voluntarily Last FDA inspection Oct 20, 2023. 6 inspections on record, 2 with serious problems.
NDC 33342-220
Memantine hydrochloride 14 mg capsule, extended release
On the label: Macleods Pharmaceuticals Limited.
Where it's made
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 14 mg
- Approval
- ANDA ANDA206310
- On the market since
- Aug 28, 2025
- Package NDCs
33342-220-0733342-220-12- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2025
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