RecallHawk

CYCLOBENZAPRINE HYDROCHLORIDE

TWI PHARMS INC

Summary

FDA approved CYCLOBENZAPRINE HYDROCHLORIDE by TWI PHARMS INC. ANDA (Generic) approval (Labeling) on 2024-12-17. CAPSULE, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA091281-16

Action Date

2024-12-17

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

CYCLOBENZAPRINE HYDROCHLORIDE, CAPSULE, EXTENDED RELEASE, ORAL. Application: ANDA091281

Context & Analysis

Frequently Asked Questions

How often does TWI PHARMS INC have FDA actions?

This is the only FDA action we have on record for TWI PHARMS INC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA091281-16" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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