RecallHawk

LISDEXAMFETAMINE DIMESYLATE

RHODES PHARMS

Summary

FDA approved LISDEXAMFETAMINE DIMESYLATE by RHODES PHARMS. ANDA (Generic) approval on 2023-08-25. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA215330-1

Action Date

2023-08-25

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

LISDEXAMFETAMINE DIMESYLATE, CAPSULE, ORAL. Application: ANDA215330

Context & Analysis

RHODES PHARMS has 13 FDA actions in our database.

Frequently Asked Questions

How often does RHODES PHARMS have FDA actions?

RHODES PHARMS has 13 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA215330-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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