Package 71610-404-60
Brand: buspirone hydrochloride
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
71610-404-60
Digits Only
7161040460
Product NDC
71610-404
Description
90 TABLET in 1 BOTTLE (71610-404-60)
Marketing
Marketing Status
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": "a93360e6-43f6-4652-a7ef-07087a718258", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["27db85e9-68ef-4d43-a319-4e2ec8dbae05"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-404-60)", "package_ndc": "71610-404-60", "marketing_start_date": "20200309"}], "brand_name": "Buspirone Hydrochloride", "product_id": "71610-404_a93360e6-43f6-4652-a7ef-07087a718258", "dosage_form": "TABLET", "product_ndc": "71610-404", "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": "ANDA208972", "marketing_category": "ANDA", "marketing_start_date": "20190417", "listing_expiration_date": "20261231"}