RecallHawk

DALFAMPRIDINE

ACTAVIS LABS FL INC

Summary

FDA approved DALFAMPRIDINE by ACTAVIS LABS FL INC. ANDA (Generic) approval (Labeling) on 2023-04-19. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA206836-4

Action Date

2023-04-19

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DALFAMPRIDINE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA206836

Context & Analysis

ACTAVIS LABS FL INC has 17 FDA actions in our database.

Frequently Asked Questions

How often does ACTAVIS LABS FL INC have FDA actions?

ACTAVIS LABS FL INC has 17 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 "ANDA206836-4" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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