Package 72789-332-60

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-332-60
Digits Only 7278933260
Product NDC 72789-332
Product ID 72789-332_401ffb0a-e4c9-09e1-e063-6294a90ade8b
Description

60 TABLET in 1 BOTTLE, PLASTIC (72789-332-60)

Marketing

Marketing Status
Marketed Since 2023-07-28
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": "401ffb0a-e4c9-09e1-e063-6294a90ade8b", "openfda": {"upc": ["0372789332604"], "unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["270398a0-21b8-407b-af76-4aeef90f72be"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-332-60)", "package_ndc": "72789-332-60", "marketing_start_date": "20230728"}], "brand_name": "Buspirone Hydrochloride", "product_id": "72789-332_401ffb0a-e4c9-09e1-e063-6294a90ade8b", "dosage_form": "TABLET", "product_ndc": "72789-332", "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": "15 mg/1"}], "application_number": "ANDA075388", "marketing_category": "ANDA", "marketing_start_date": "20200727", "listing_expiration_date": "20261231"}