Package 71610-206-30

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71610-206-30
Digits Only 7161020630
Product NDC 71610-206
Product ID 71610-206_636c7482-d41f-4a26-a55c-183f4169c148
Description

30 TABLET in 1 BOTTLE (71610-206-30)

Marketing

Marketing Status
Marketed Since 2018-12-13
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": "636c7482-d41f-4a26-a55c-183f4169c148", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["310c6bea-838b-43e4-87e0-a0050829c242"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71610-206-30)", "package_ndc": "71610-206-30", "marketing_start_date": "20181213"}], "brand_name": "Buspirone hydrochloride", "product_id": "71610-206_636c7482-d41f-4a26-a55c-183f4169c148", "dosage_form": "TABLET", "product_ndc": "71610-206", "generic_name": "Buspirone hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20140503", "listing_expiration_date": "20261231"}