NDC 75907-050
Methylphenidate Hydrochloride (LA) 20 mg capsule, extended release
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Dr. Reddy's Laboratories Inc. names for other drugs.
Product details
- Generic drug
- Methylphenidate: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078458
- On the market since
- Dec 20, 2024
- Package NDCs
75907-050-01- Official label
- DailyMed (National Library of Medicine), updated Sep 30, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?