RecallHawk

FLUTICASONE PROPIONATE

CHARTWELL RX

Summary

FDA approved FLUTICASONE PROPIONATE by CHARTWELL RX. ANDA (Generic) approval (Labeling) on 2023-08-08. OINTMENT, TOPICAL.

Details

Source

Drug Approval

External ID

ANDA076300-7

Action Date

2023-08-08

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

FLUTICASONE PROPIONATE, OINTMENT, TOPICAL. Application: ANDA076300

Context & Analysis

CHARTWELL RX has 64 FDA actions in our database.

Frequently Asked Questions

How often does CHARTWELL RX have FDA actions?

CHARTWELL RX has 64 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 "ANDA076300-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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