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 33342-298
Memantine Hydrochloride 10 mg tablet
On the label: Macleods Pharmaceuticals Limited.
Where it's made
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA202840
- On the market since
- Oct 13, 2015
- Package NDCs
33342-298-0933342-298-1233342-298-15- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2022
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