Package 82868-082-30
Brand: buspirone hcl
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
82868-082-30
Digits Only
8286808230
Product NDC
82868-082
Description
30 TABLET in 1 BOTTLE, PLASTIC (82868-082-30)
Marketing
Marketing Status
Brand
buspirone hcl
Generic
buspirone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "472049db-f1eb-5e2b-e063-6294a90a2ff8", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["472049d2-c4d9-5a38-e063-6294a90a5cf1"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-082-30)", "package_ndc": "82868-082-30", "marketing_start_date": "20250619"}], "brand_name": "busPIRone HCl", "product_id": "82868-082_472049db-f1eb-5e2b-e063-6294a90a2ff8", "dosage_form": "TABLET", "product_ndc": "82868-082", "generic_name": "buspirone hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "busPIRone HCl", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA075521", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}