Package 0093-5200-06

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-5200-06
Digits Only 0093520006
Product NDC 0093-5200
Product ID 0093-5200_f2a05d58-ca70-4b89-aa19-6b63e85a57a5
Description

60 TABLET in 1 BOTTLE (0093-5200-06)

Marketing

Marketing Status
Marketed Since 2004-03-26
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Buspirone Hydrochloride ndc-match (0.95)

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": "500 TABLET in 1 BOTTLE (0093-5200-05)", "package_ndc": "0093-5200-05", "marketing_start_date": "20040326"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (0093-5200-06)", "package_ndc": "0093-5200-06", "marketing_start_date": "20040326"}], "brand_name": "Buspirone Hydrochloride", "product_id": "0093-5200_f2a05d58-ca70-4b89-aa19-6b63e85a57a5", "dosage_form": "TABLET", "product_ndc": "0093-5200", "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": "30 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}