RecallHawk

DICLOFENAC POTASSIUM (DICLOFENAC POTASSIUM TABLETS)

UMEDICA

Summary

FDA approved DICLOFENAC POTASSIUM (DICLOFENAC POTASSIUM TABLETS) by UMEDICA. ANDA (Generic) approval (Manufacturing (CMC)) on 2025-06-30. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA215750-8

Action Date

2025-06-30

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DICLOFENAC POTASSIUM (generic: DICLOFENAC POTASSIUM TABLETS), TABLET, ORAL. Application: ANDA215750

Company

Context & Analysis

UMEDICA has 6 FDA actions in our database.

Frequently Asked Questions

How often does UMEDICA have FDA actions?

UMEDICA has 6 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 "ANDA215750-8" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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