RecallHawk

DEXAMETHASONE

KANCHAN HLTHCARE

Summary

FDA approved DEXAMETHASONE by KANCHAN HLTHCARE. ANDA (Generic) approval (Labeling) on 2024-06-05. ELIXIR, ORAL.

Details

Source

Drug Approval

External ID

ANDA084754-61

Action Date

2024-06-05

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DEXAMETHASONE, ELIXIR, ORAL. Application: ANDA084754

Context & Analysis

KANCHAN HLTHCARE has 2 FDA actions in our database.

Frequently Asked Questions

How often does KANCHAN HLTHCARE have FDA actions?

KANCHAN HLTHCARE has 2 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 "ANDA084754-61" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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