RecallHawk

BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE)

SINOTHERAPEUTICS INC

Summary

FDA approved BUPROPION HYDROCHLORIDE (XL) (BUPROPION HYDROCHLORIDE) by SINOTHERAPEUTICS INC. ANDA (Generic) approval (Labeling) on 2024-12-17. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA208652-12

Action Date

2024-12-17

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BUPROPION HYDROCHLORIDE (XL) (generic: BUPROPION HYDROCHLORIDE), TABLET, EXTENDED RELEASE, ORAL. Application: ANDA208652

Context & Analysis

SINOTHERAPEUTICS INC has 3 FDA actions in our database.

Frequently Asked Questions

How often does SINOTHERAPEUTICS INC have FDA actions?

SINOTHERAPEUTICS INC has 3 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 "ANDA208652-12" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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