RecallHawk

SODIUM PHENYLBUTYRATE

GLENMARK PHARMS LTD

Summary

FDA approved SODIUM PHENYLBUTYRATE by GLENMARK PHARMS LTD. ANDA (Generic) approval on 2022-11-01. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA216462-1

Action Date

2022-11-01

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

SODIUM PHENYLBUTYRATE, TABLET, ORAL. Application: ANDA216462

Context & Analysis

GLENMARK PHARMS LTD has 36 FDA actions in our database.

Frequently Asked Questions

How often does GLENMARK PHARMS LTD have FDA actions?

GLENMARK PHARMS LTD has 36 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 "ANDA216462-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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