Package 70518-0380-0
Brand: buspirone hydrochloride
Generic: buspirone hydrochloridePackage Facts
Identity
Package NDC
70518-0380-0
Digits Only
7051803800
Product NDC
70518-0380
Description
30 TABLET in 1 BLISTER PACK (70518-0380-0)
Marketing
Marketing Status
Brand
buspirone hydrochloride
Generic
buspirone hydrochloride
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b4cb86d-e507-3651-e063-6394a90a8848", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["7ac98a7f-0ded-427f-899a-c3f6d1997403"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0380-0)", "package_ndc": "70518-0380-0", "marketing_start_date": "20170403"}], "brand_name": "Buspirone hydrochloride", "product_id": "70518-0380_2b4cb86d-e507-3651-e063-6394a90a8848", "dosage_form": "TABLET", "product_ndc": "70518-0380", "generic_name": "Buspirone hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20170403", "listing_expiration_date": "20261231"}