Package 72162-2304-0

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 72162-2304-0
Digits Only 7216223040
Product NDC 72162-2304
Product ID 72162-2304_250c155b-3d38-41f9-945b-e983a206e583
Description

1000 CAPSULE in 1 BOTTLE (72162-2304-0)

Marketing

Marketing Status
Marketed Since 2024-04-30
Brand pregabalin
Generic pregabalin
Sample Package No

Linked Drug Pages (1)

PREGABALIN ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "250c155b-3d38-41f9-945b-e983a206e583", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483440"], "spl_set_id": ["335e3bcb-10a3-481b-ad95-ee9ceaa3689e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72162-2304-0)", "package_ndc": "72162-2304-0", "marketing_start_date": "20240430"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72162-2304-9)", "package_ndc": "72162-2304-9", "marketing_start_date": "20240430"}], "brand_name": "PREGABALIN", "product_id": "72162-2304_250c155b-3d38-41f9-945b-e983a206e583", "dosage_form": "CAPSULE", "product_ndc": "72162-2304", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "150 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}