Package 71335-2820-1

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2820-1
Digits Only 7133528201
Product NDC 71335-2820
Product ID 71335-2820_2dcf0b87-6917-4c75-ae93-c27bf9344c12
Description

100 TABLET in 1 BOTTLE (71335-2820-1)

Marketing

Marketing Status
Marketed Since 2025-11-10
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": "2dcf0b87-6917-4c75-ae93-c27bf9344c12", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["8c811d3a-8b2d-44f5-bc8f-8eb563f18c3f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2820-1)", "package_ndc": "71335-2820-1", "marketing_start_date": "20251110"}], "brand_name": "Buspirone hydrochloride", "product_id": "71335-2820_2dcf0b87-6917-4c75-ae93-c27bf9344c12", "dosage_form": "TABLET", "product_ndc": "71335-2820", "generic_name": "Buspirone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA078888", "marketing_category": "ANDA", "marketing_start_date": "20230321", "listing_expiration_date": "20261231"}