Package 72789-181-90

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-181-90
Digits Only 7278918190
Product NDC 72789-181
Product ID 72789-181_4019e519-dc9e-1fc4-e063-6294a90a8865
Description

90 TABLET in 1 BOTTLE, PLASTIC (72789-181-90)

Marketing

Marketing Status
Marketed Since 2021-04-13
Brand buspirone hydrochloride
Generic buspirone hydrochloride
Sample Package No

Linked Drug Pages (1)

Buspirone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4019e519-dc9e-1fc4-e063-6294a90a8865", "openfda": {"upc": ["0372789181905"], "unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["b217f341-7d51-475d-887f-f16786164c7b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-181-90)", "package_ndc": "72789-181-90", "marketing_start_date": "20210413"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72789-181_4019e519-dc9e-1fc4-e063-6294a90a8865", "dosage_form": "TABLET", "product_ndc": "72789-181", "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": "10 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}