Package 69584-092-10

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69584-092-10
Digits Only 6958409210
Product NDC 69584-092
Description

100 TABLET in 1 BOTTLE (69584-092-10)

Marketing

Marketing Status
Marketed Since 2020-07-27
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": "8c9f66ca-78a9-418c-b11e-ba4391843257", "openfda": {"upc": ["0369584093502"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["97fcebc1-6615-4b9d-b0f3-6434850f407c"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69584-092-10)", "package_ndc": "69584-092-10", "marketing_start_date": "20200727"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69584-092-50)", "package_ndc": "69584-092-50", "marketing_start_date": "20200727"}], "brand_name": "Buspirone Hydrochloride", "product_id": "69584-092_8c9f66ca-78a9-418c-b11e-ba4391843257", "dosage_form": "TABLET", "product_ndc": "69584-092", "generic_name": "buspirone hydrochloride", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}