Package 70518-2980-0

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 70518-2980-0
Digits Only 7051829800
Product NDC 70518-2980
Product ID 70518-2980_4abb620f-2f08-605d-e063-6394a90a9a7e
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2980-0)

Marketing

Marketing Status
Marketed Since 2021-01-06
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": "4abb620f-2f08-605d-e063-6394a90a9a7e", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["577127"], "spl_set_id": ["9111d695-9f3a-4b07-9daa-c1339b16acb3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2980-0)", "package_ndc": "70518-2980-0", "marketing_start_date": "20210106"}], "brand_name": "Pregabalin", "product_id": "70518-2980_4abb620f-2f08-605d-e063-6394a90a9a7e", "dosage_form": "CAPSULE", "product_ndc": "70518-2980", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "225 mg/1"}], "application_number": "ANDA209743", "marketing_category": "ANDA", "marketing_start_date": "20210106", "listing_expiration_date": "20271231"}