Apl Healthcare Limited
Tirupati, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Dec 17, 2025. 5 inspections on record.
NDC 59651-404
Memantine Hydrochloride 7 mg capsule, extended release
On the label: Aurobindo Pharma Limited.
Where it's made
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 7 mg
- Approval
- ANDA ANDA214651
- On the market since
- Aug 9, 2021
- Package NDCs
59651-404-3059651-404-90- Official label
- DailyMed (National Library of Medicine), updated Nov 5, 2022
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