Package 72189-200-82

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-200-82
Digits Only 7218920082
Product NDC 72189-200
Description

180 TABLET in 1 BOTTLE (72189-200-82)

Marketing

Marketing Status
Marketed Since 2021-04-12
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": "4c498a8f-f65a-5df5-e063-6394a90ae0fd", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866083"], "spl_set_id": ["bae98d45-e192-56e3-e053-2a95a90aadc3"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (72189-200-82)", "package_ndc": "72189-200-82", "marketing_start_date": "20210412"}], "brand_name": "BUSPIRONE HYDROCHLORIDE", "product_id": "72189-200_4c498a8f-f65a-5df5-e063-6394a90ae0fd", "dosage_form": "TABLET", "product_ndc": "72189-200", "generic_name": "BUSPIRONE HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUSPIRONE HYDROCHLORIDE", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA202330", "marketing_category": "ANDA", "marketing_start_date": "20210412", "listing_expiration_date": "20271231"}