Package 70518-3643-0

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 70518-3643-0
Digits Only 7051836430
Product NDC 70518-3643
Product ID 70518-3643_43d05ca9-55c9-c3e9-e063-6394a90a7364
Description

90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3643-0)

Marketing

Marketing Status
Marketed Since 2023-02-15
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": "43d05ca9-55c9-c3e9-e063-6394a90a7364", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483438"], "spl_set_id": ["3c8ea6da-5771-4096-a915-700e51ced05c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3643-0)", "package_ndc": "70518-3643-0", "marketing_start_date": "20230215"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE, PLASTIC (70518-3643-1)", "package_ndc": "70518-3643-1", "marketing_start_date": "20230215"}], "brand_name": "Pregabalin", "product_id": "70518-3643_43d05ca9-55c9-c3e9-e063-6394a90a7364", "dosage_form": "CAPSULE", "product_ndc": "70518-3643", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "100 mg/1"}], "application_number": "ANDA207799", "marketing_category": "ANDA", "marketing_start_date": "20230215", "listing_expiration_date": "20261231"}