Package 80425-0027-1

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 80425-0027-1
Digits Only 8042500271
Product NDC 80425-0027
Product ID 80425-0027_2a987953-08cf-1c4c-e063-6394a90a5a82
Description

60 CAPSULE in 1 BOTTLE (80425-0027-1)

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": "2a987953-08cf-1c4c-e063-6394a90a5a82", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483448"], "spl_set_id": ["afc8d9f1-df31-607b-e053-2995a90a028c"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (80425-0027-1)", "package_ndc": "80425-0027-1", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "80425-0027_2a987953-08cf-1c4c-e063-6394a90a5a82", "dosage_form": "CAPSULE", "product_ndc": "80425-0027", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "50 mg/1"}], "application_number": "ANDA210432", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}