23594-152 : Exxua 54.5 mg Oral Tablet, Extended Release


NDC: 23594-152
Labeler: Aytu Therapeutics, LLC
Product Type: Human Prescription Drug
Drug Name:  Exxua
Dosage Form: Oral Tablet, Extended Release
Application #: NDA021164
Rev. Date: 


NDC Package Codes:

  • 23594-152-30: 30 TABLET, EXTENDED RELEASE IN 1 BOTTLE (23594‑152‑30)

Active Ingredients:

  • Gepirone Hydrochloride

Dosage Strength:

  • 54.5 mg

Related Products:

Based on records with the same trade name.
  • 23594-150 Exxua 18.2 mg Oral Tablet, Extended Release by Aytu Therapeutics, LLC
  • 23594-151 Exxua 36.3 mg Oral Tablet, Extended Release by Aytu Therapeutics, LLC
  • 23594-153 Exxua 72.6 mg Oral Tablet, Extended Release by Aytu Therapeutics, LLC
  • 83504-150 Exxua 18.2 mg Oral Tablet, Delayed Release by Fabre Kramer Pharmaceuticals, Inc.
  • 83504-151 Exxua 36.3 mg Oral Tablet, Delayed Release by Fabre Kramer Pharmaceuticals, Inc.
  • 83504-152 Exxua 54.5 mg Oral Tablet, Delayed Release by Fabre Kramer Pharmaceuticals, Inc.
  • 83504-153 Exxua 72.6 mg Oral Tablet, Delayed Release by Fabre Kramer Pharmaceuticals, Inc.

NDC QR Code

Scan the QR code below to easily reference this data in the future:

NDC 23594-152 QR Code

< Prev: 23594-151Next: 23594-153 >




Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.