Package 80425-0030-2

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 80425-0030-2
Digits Only 8042500302
Product NDC 80425-0030
Product ID 80425-0030_43ccc5cb-7aee-4ee0-e063-6294a90af140
Description

90 CAPSULE in 1 BOTTLE (80425-0030-2)

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": "43ccc5cb-7aee-4ee0-e063-6294a90af140", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483450"], "spl_set_id": ["afc89689-bea9-92ec-e053-2995a90a7f21"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (80425-0030-1)", "package_ndc": "80425-0030-1", "marketing_start_date": "20190719"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (80425-0030-2)", "package_ndc": "80425-0030-2", "marketing_start_date": "20190719"}], "brand_name": "Pregabalin", "product_id": "80425-0030_43ccc5cb-7aee-4ee0-e063-6294a90af140", "dosage_form": "CAPSULE", "product_ndc": "80425-0030", "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": "75 mg/1"}], "application_number": "ANDA209357", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}