Package 80425-0170-3

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 80425-0170-3
Digits Only 8042501703
Product NDC 80425-0170
Product ID 80425-0170_2a99a80e-d071-27e6-e063-6294a90ae0fe
Description

90 CAPSULE in 1 BOTTLE (80425-0170-3)

Marketing

Marketing Status
Marketed Since 2019-10-08
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": "2a99a80e-d071-27e6-e063-6294a90ae0fe", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438"], "spl_set_id": ["c8bfc4f9-6208-4eaa-e053-2a95a90ada97"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (80425-0170-3)", "package_ndc": "80425-0170-3", "marketing_start_date": "20191008"}], "brand_name": "Pregabalin", "product_id": "80425-0170_2a99a80e-d071-27e6-e063-6294a90ae0fe", "dosage_form": "CAPSULE", "product_ndc": "80425-0170", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "100 mg/1"}], "application_number": "ANDA206912", "marketing_category": "ANDA", "marketing_start_date": "20191008", "listing_expiration_date": "20261231"}