Package 0093-0053-01

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-0053-01
Digits Only 0093005301
Product NDC 0093-0053
Description

100 TABLET in 1 BOTTLE (0093-0053-01)

Marketing

Marketing Status
Marketed Since 2002-02-28
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": "f2a05d58-ca70-4b89-aa19-6b63e85a57a5", "openfda": {"upc": ["0300930054013"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["6fac36b4-b223-479e-913f-f8c9cdb9e119"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0093-0053-01)", "package_ndc": "0093-0053-01", "marketing_start_date": "20020228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0093-0053-05)", "package_ndc": "0093-0053-05", "marketing_start_date": "20020301"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0093-0053_f2a05d58-ca70-4b89-aa19-6b63e85a57a5", "dosage_form": "TABLET", "product_ndc": "0093-0053", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020228", "listing_expiration_date": "20261231"}