Package 80425-0123-3

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 80425-0123-3
Digits Only 8042501233
Product NDC 80425-0123
Product ID 80425-0123_2a99a80e-d06b-27e6-e063-6294a90ae0fe
Description

90 CAPSULE in 1 BOTTLE (80425-0123-3)

Marketing

Marketing Status
Marketed Since 2019-07-19
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-d06b-27e6-e063-6294a90ae0fe", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438"], "spl_set_id": ["b817083c-b535-2269-e053-2a95a90af5b9"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (80425-0123-3)", "package_ndc": "80425-0123-3", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "80425-0123_2a99a80e-d06b-27e6-e063-6294a90ae0fe", "dosage_form": "CAPSULE", "product_ndc": "80425-0123", "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": "ANDA209743", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}