Package 0615-8527-39

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8527-39
Digits Only 0615852739
Product NDC 0615-8527
Description

30 TABLET in 1 BLISTER PACK (0615-8527-39)

Marketing

Marketing Status
Marketed Since 2024-09-18
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1999411b-cc4c-4dac-a2de-c3a4dacfa1d5", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866090"], "spl_set_id": ["d5fcc60d-5465-4075-948c-1aa4ff21af4c"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8527-39)", "package_ndc": "0615-8527-39", "marketing_start_date": "20240918"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0615-8527_1999411b-cc4c-4dac-a2de-c3a4dacfa1d5", "dosage_form": "TABLET", "product_ndc": "0615-8527", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}