Package 68071-3834-3

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3834-3
Digits Only 6807138343
Product NDC 68071-3834
Product ID 68071-3834_335107d2-e2ba-835d-e063-6394a90a9142
Description

30 TABLET in 1 BOTTLE, PLASTIC (68071-3834-3)

Marketing

Marketing Status
Marketed Since 2025-04-21
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": "335107d2-e2ba-835d-e063-6394a90a9142", "openfda": {"upc": ["0368071383430"], "unii": ["207LT9J9OC"], "rxcui": ["866018"], "spl_set_id": ["335107c9-5799-c4df-e063-6294a90a5ca0"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-3834-3)", "package_ndc": "68071-3834-3", "marketing_start_date": "20250421"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68071-3834_335107d2-e2ba-835d-e063-6394a90a9142", "dosage_form": "TABLET", "product_ndc": "68071-3834", "generic_name": "Buspirone Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buspirone Hydrochloride", "active_ingredients": [{"name": "BUSPIRONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20231017", "listing_expiration_date": "20261231"}