Aurobindo Pharma Limited
Mahabubnagar, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection May 10, 2022. 7 inspections on record, 1 with serious problems.
NDC 65862-653
Memantine Hydrochloride 10 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA203175
- On the market since
- Oct 13, 2015
- Package NDCs
65862-653-0365862-653-1065862-653-6065862-653-7865862-653-99- Official label
- DailyMed (National Library of Medicine), updated Nov 8, 2022
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