Package 71610-291-60

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-291-60
Digits Only 7161029160
Product NDC 71610-291
Description

90 TABLET in 1 BOTTLE (71610-291-60)

Marketing

Marketing Status
Marketed Since 2019-06-05
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": "ab84266e-acad-41f9-ada7-9a54817dd289", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["e2c672b3-6130-4dd1-8066-0ce9451cb8c7"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-291-60)", "package_ndc": "71610-291-60", "marketing_start_date": "20190605"}], "brand_name": "BusPIRone Hydrochloride", "product_id": "71610-291_ab84266e-acad-41f9-ada7-9a54817dd289", "dosage_form": "TABLET", "product_ndc": "71610-291", "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": "ANDA209696", "marketing_category": "ANDA", "marketing_start_date": "20180703", "listing_expiration_date": "20261231"}