Package 72888-049-30

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 72888-049-30
Digits Only 7288804930
Product NDC 72888-049
Product ID 72888-049_49fe33c0-b2ae-e0c1-e063-6294a90a36a4
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-049-30)

Marketing

Marketing Status
Marketed Since 2022-03-22
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": "49fe33c0-b2ae-e0c1-e063-6294a90a36a4", "openfda": {"upc": ["0372888049304", "0372888051307", "0372888050300"], "unii": ["55JG375S6M"], "rxcui": ["1988974", "1988977", "1988980"], "spl_set_id": ["2ffee7e7-bfa0-4933-9baf-7df55080816e"], "manufacturer_name": ["Advagen Pharma Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72888-049-30)", "package_ndc": "72888-049-30", "marketing_start_date": "20220322"}], "brand_name": "Pregabalin", "product_id": "72888-049_49fe33c0-b2ae-e0c1-e063-6294a90a36a4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "72888-049", "dea_schedule": "CV", "generic_name": "Pregabalin", "labeler_name": "Advagen Pharma Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "82.5 mg/1"}], "application_number": "ANDA215249", "marketing_category": "ANDA", "marketing_start_date": "20220322", "listing_expiration_date": "20271231"}