RecallHawk

DROXIDOPA

ADAPTIS

Summary

FDA approved DROXIDOPA by ADAPTIS. ANDA (Generic) approval on 2021-11-01. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA215265-1

Action Date

2021-11-01

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DROXIDOPA, CAPSULE, ORAL. Application: ANDA215265

Company

Context & Analysis

ADAPTIS has 6 FDA actions in our database.

Frequently Asked Questions

How often does ADAPTIS have FDA actions?

ADAPTIS 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 "ANDA215265-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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