Package 72162-1541-4

Brand: pregabalin

Generic: pregabalin
NDC Package

Package Facts

Identity

Package NDC 72162-1541-4
Digits Only 7216215414
Product NDC 72162-1541
Product ID 72162-1541_7e224ba4-8a31-4aaf-ad7c-6af62116c310
Description

90 CAPSULE in 1 BOTTLE (72162-1541-4)

Marketing

Marketing Status
Marketed Since 2024-08-12
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": "7e224ba4-8a31-4aaf-ad7c-6af62116c310", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["483442"], "spl_set_id": ["90b65884-4222-4011-b042-88b83e51c57a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (72162-1541-4)", "package_ndc": "72162-1541-4", "marketing_start_date": "20240812"}], "brand_name": "Pregabalin", "product_id": "72162-1541_7e224ba4-8a31-4aaf-ad7c-6af62116c310", "dosage_form": "CAPSULE", "product_ndc": "72162-1541", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pregabalin", "active_ingredients": [{"name": "PREGABALIN", "strength": "25 mg/1"}], "application_number": "ANDA208677", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20261231"}