Package 72205-077-30

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 72205-077-30
Digits Only 7220507730
Product NDC 72205-077
Product ID 72205-077_f6aa5977-97c8-4a56-8e35-d9ab5cc24369
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-077-30)

Marketing

Marketing Status
Marketed Since 2021-04-13
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": "f6aa5977-97c8-4a56-8e35-d9ab5cc24369", "openfda": {"upc": ["0372205078307", "0372205077300", "0372205079304"], "unii": ["55JG375S6M"], "rxcui": ["1988974", "1988977", "1988980"], "spl_set_id": ["f6aa5977-97c8-4a56-8e35-d9ab5cc24369"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72205-077-30)", "package_ndc": "72205-077-30", "marketing_start_date": "20210413"}], "brand_name": "PREGABALIN", "product_id": "72205-077_f6aa5977-97c8-4a56-8e35-d9ab5cc24369", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "72205-077", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PREGABALIN", "active_ingredients": [{"name": "PREGABALIN", "strength": "82.5 mg/1"}], "application_number": "ANDA213226", "marketing_category": "ANDA", "marketing_start_date": "20210413", "listing_expiration_date": "20261231"}