Package 71610-183-60

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-183-60
Digits Only 7161018360
Product NDC 71610-183
Description

90 TABLET in 1 BOTTLE (71610-183-60)

Marketing

Marketing Status
Marketed Since 2018-10-31
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": "0e7eed66-f0af-469e-ad79-8d442af82177", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["b7e3a98c-9ec5-4c21-9218-0d53a555a75c"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-183-60)", "package_ndc": "71610-183-60", "marketing_start_date": "20181031"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71610-183_0e7eed66-f0af-469e-ad79-8d442af82177", "dosage_form": "TABLET", "product_ndc": "71610-183", "generic_name": "Buspirone Hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA075022", "marketing_category": "ANDA", "marketing_start_date": "20020301", "listing_expiration_date": "20261231"}