Drugplain

Methylphenidate Hydrochloride (LA) 10 mg/1

Methylphenidate Hydrochloride · CAPSULE, EXTENDED RELEASE · Dr. Reddy's Laboratories Inc

No Recall HistoryCurrently in Shortage
Plain English

Methylphenidate Hydrochloride (LA) is a capsule, extended release containing methylphenidate hydrochloride at 10 mg/1, taken oral. Manufactured by Dr. Reddy's Laboratories Inc.

Key Facts

Brand Name
Methylphenidate Hydrochloride (LA)
Generic Name
Methylphenidate Hydrochloride
NDC Code (Product)
75907-049
Manufacturer
Dr. Reddy's Laboratories Inc
Strength
10 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
DEA Schedule
Schedule II (Controlled)
Application #
ANDA200886
Marketing Start
12/20/2024

Recall History

No Recall History

Frequently Asked Questions

What is Methylphenidate Hydrochloride (LA) used for?

Methylphenidate Hydrochloride (LA) contains Methylphenidate Hydrochloride. It is a capsule, extended release taken oral. Consult your doctor for specific uses.

Is Methylphenidate Hydrochloride (LA) a controlled substance?

Yes, Methylphenidate Hydrochloride (LA) is classified as CII under the DEA Controlled Substances Act.

What is the generic name for Methylphenidate Hydrochloride (LA)?

The generic name for Methylphenidate Hydrochloride (LA) is Methylphenidate Hydrochloride. There are 12 other brand versions of Methylphenidate Hydrochloride.

What is the NDC code for Methylphenidate Hydrochloride (LA) 10 mg/1?

The NDC (National Drug Code) for Methylphenidate Hydrochloride (LA) 10 mg/1 is 75907-049, listed by Dr. Reddy's Laboratories Inc.

Product NDC

75907-049

Package NDC

75907-049-01

Other Methylphenidate Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)