Package 80425-0160-3

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 80425-0160-3
Digits Only 8042501603
Product NDC 80425-0160
Description

90 CAPSULE in 1 BOTTLE (80425-0160-3)

Marketing

Marketing Status
Marketed Since 2019-07-21
Brand pregabalin
Generic pregabalin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99c981-daee-71e5-e063-6294a90a5c1d", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483444"], "spl_set_id": ["c89a3514-f637-e54f-e053-2a95a90a6881"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (80425-0160-3)", "package_ndc": "80425-0160-3", "marketing_start_date": "20190721"}], "brand_name": "Pregabalin", "product_id": "80425-0160_2a99c981-daee-71e5-e063-6294a90a5c1d", "dosage_form": "CAPSULE", "product_ndc": "80425-0160", "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": "300 mg/1"}], "application_number": "ANDA207799", "marketing_category": "ANDA", "marketing_start_date": "20190721", "listing_expiration_date": "20261231"}