Package 68071-2995-3

Brand: buspirone hydrochloride

Generic: buspirone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-2995-3
Digits Only 6807129953
Product NDC 68071-2995
Product ID 68071-2995_2d53e84a-506a-e4c8-e063-6294a90a3f8d
Description

30 TABLET in 1 BOTTLE, PLASTIC (68071-2995-3)

Marketing

Marketing Status
Marketed Since 2023-05-16
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": "2d53e84a-506a-e4c8-e063-6294a90a3f8d", "openfda": {"upc": ["0368071299533"], "unii": ["207LT9J9OC"], "rxcui": ["866094"], "spl_set_id": ["fbd7f3fa-11f8-a319-e053-6294a90acae4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68071-2995-3)", "package_ndc": "68071-2995-3", "marketing_start_date": "20230516"}], "brand_name": "Buspirone Hydrochloride", "product_id": "68071-2995_2d53e84a-506a-e4c8-e063-6294a90a3f8d", "dosage_form": "TABLET", "product_ndc": "68071-2995", "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": "5 mg/1"}], "application_number": "ANDA210907", "marketing_category": "ANDA", "marketing_start_date": "20191114", "listing_expiration_date": "20261231"}