Package 72189-019-82

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 72189-019-82
Digits Only 7218901982
Product NDC 72189-019
Product ID 72189-019_2c4e85d7-3b08-6b90-e063-6294a90a0ea8
Description

180 CAPSULE in 1 BOTTLE (72189-019-82)

Marketing

Marketing Status
Marketed Since 2019-07-31
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": "2c4e85d7-3b08-6b90-e063-6294a90a0ea8", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483448"], "spl_set_id": ["8efb9652-86b9-4cb5-e053-2995a90adac0"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "180 CAPSULE in 1 BOTTLE (72189-019-82)", "package_ndc": "72189-019-82", "marketing_start_date": "20190731"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72189-019-90)", "package_ndc": "72189-019-90", "marketing_start_date": "20190731"}], "brand_name": "PREGABALIN", "product_id": "72189-019_2c4e85d7-3b08-6b90-e063-6294a90a0ea8", "dosage_form": "CAPSULE", "product_ndc": "72189-019", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "50 mg/1"}], "application_number": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20190731", "listing_expiration_date": "20261231"}