Package 42806-665-60
Brand: buspirone hydrochloride
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
42806-665-60
Digits Only
4280666560
Product NDC
42806-665
Description
60 TABLET in 1 BOTTLE (42806-665-60)
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": "ac140e7e-3d5b-4329-8e3e-e21be7417fed", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["e8f43c66-f8de-419f-9ea9-43ddc4ec0798"], "manufacturer_name": ["EPIC PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (42806-665-60)", "package_ndc": "42806-665-60", "marketing_start_date": "20200619"}], "brand_name": "Buspirone hydrochloride", "product_id": "42806-665_ac140e7e-3d5b-4329-8e3e-e21be7417fed", "dosage_form": "TABLET", "product_ndc": "42806-665", "generic_name": "Buspirone hydrochloride", "labeler_name": "EPIC PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202087", "marketing_category": "ANDA", "marketing_start_date": "20200619", "listing_expiration_date": "20261231"}