Sun Pharmaceutical Industries Limited
Dadra, India · makes it, tests it, packages it and labels it
Problems found, fixed voluntarily Last FDA inspection Mar 29, 2019. 5 inspections on record.
NDC 47335-033
memantine hydrochloride 21 mg capsule, extended release
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- capsule, extended release
- Strength
- 21 mg
- Approval
- ANDA ANDA205905
- On the market since
- Jun 14, 2013
- Package NDCs
47335-033-1847335-033-8147335-033-83- Official label
- DailyMed (National Library of Medicine), updated Dec 27, 2019
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