Package 72789-142-60
Brand: buspirone hydrochloride
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
72789-142-60
Digits Only
7278914260
Product NDC
72789-142
Description
60 TABLET in 1 BOTTLE, PLASTIC (72789-142-60)
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": "4b96ead2-cbe0-fb3c-e063-6294a90ad561", "openfda": {"upc": ["0372789141015", "0372789140018", "0372789139012", "0372789142609"], "unii": ["207LT9J9OC"], "rxcui": ["866018", "866083", "866090", "866094"], "spl_set_id": ["476f4f55-c6c1-4f39-950e-59236f499577"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-142-01)", "package_ndc": "72789-142-01", "marketing_start_date": "20201106"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-142-60)", "package_ndc": "72789-142-60", "marketing_start_date": "20240510"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72789-142_4b96ead2-cbe0-fb3c-e063-6294a90ad561", "dosage_form": "TABLET", "product_ndc": "72789-142", "generic_name": "buspirone hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA078302", "marketing_category": "ANDA", "marketing_start_date": "20200501", "listing_expiration_date": "20271231"}