Package 72162-2199-1

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2199-1
Digits Only 7216221991
Product NDC 72162-2199
Product ID 72162-2199_9215bf81-1137-4e26-989d-a52124afbff9
Description

100 TABLET in 1 BOTTLE (72162-2199-1)

Marketing

Marketing Status
Marketed Since 2023-12-15
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": "9215bf81-1137-4e26-989d-a52124afbff9", "openfda": {"unii": ["207LT9J9OC"], "rxcui": ["866111"], "spl_set_id": ["b07c0a91-892c-47f5-819e-a128e0ef1ed7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2199-1)", "package_ndc": "72162-2199-1", "marketing_start_date": "20231215"}], "brand_name": "Buspirone hydrochloride", "product_id": "72162-2199_9215bf81-1137-4e26-989d-a52124afbff9", "dosage_form": "TABLET", "product_ndc": "72162-2199", "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"}