Package 71610-608-60

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-608-60
Digits Only 7161060860
Product NDC 71610-608
Description

90 TABLET in 1 BOTTLE (71610-608-60)

Marketing

Marketing Status
Marketed Since 2021-10-26
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": "2d05f5d2-27b7-413b-bd6c-43d3e047e38a", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["62e4345a-2c51-4f93-89f0-282895ced785"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-608-60)", "package_ndc": "71610-608-60", "marketing_start_date": "20211026"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71610-608_2d05f5d2-27b7-413b-bd6c-43d3e047e38a", "dosage_form": "TABLET", "product_ndc": "71610-608", "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": "7.5 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20170217", "listing_expiration_date": "20261231"}