Package 23594-152-30

Brand: exxua

Generic: gepirone
NDC Package

Package Facts

Identity

Package NDC 23594-152-30
Digits Only 2359415230
Product NDC 23594-152
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (23594-152-30)

Marketing

Marketing Status
Marketed Since 2025-10-01
Brand exxua
Generic gepirone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "414d62f1-85aa-cfa6-e063-6394a90a69fc", "openfda": {"upc": ["0323594150303", "0323594152307", "0323594153304", "0323594151300"], "unii": ["80C9L8EP6V"], "rxcui": ["2672372", "2672379", "2672382", "2672385", "2672388", "2672391", "2672394", "2672397", "2732202", "2732203"], "spl_set_id": ["0c78edd8-6acb-433c-9d34-2527da8d64e1"], "manufacturer_name": ["Aytu Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (23594-152-30)", "package_ndc": "23594-152-30", "marketing_start_date": "20251001"}], "brand_name": "EXXUA", "product_id": "23594-152_414d62f1-85aa-cfa6-e063-6394a90a69fc", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "23594-152", "generic_name": "gepirone", "labeler_name": "Aytu Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EXXUA", "active_ingredients": [{"name": "GEPIRONE HYDROCHLORIDE", "strength": "54.5 mg/1"}], "application_number": "NDA021164", "marketing_category": "NDA", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}