Package 61919-166-60
Brand: buspirone hydrochloride
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
61919-166-60
Digits Only
6191916660
Product NDC
61919-166
Description
60 TABLET in 1 BOTTLE (61919-166-60)
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": "47e15246-5edb-3524-e063-6294a90a3fd4", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["8e9c0553-c994-f54a-e053-2a95a90a6fa3"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-166-60)", "package_ndc": "61919-166-60", "marketing_start_date": "20190726"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "61919-166_47e15246-5edb-3524-e063-6294a90a3fd4", "dosage_form": "TABLET", "product_ndc": "61919-166", "generic_name": "BUSPIRONE HYDROCHLORIDE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUSPIRONE HYDROCHLORIDE", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202557", "marketing_category": "ANDA", "marketing_start_date": "20190726", "listing_expiration_date": "20271231"}