Package 58151-245-93
Brand: lyrica cr
Generic: pregabalinPackage Facts
Identity
Package NDC
58151-245-93
Digits Only
5815124593
Product NDC
58151-245
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58151-245-93)
Marketing
Marketing Status
Brand
lyrica cr
Generic
pregabalin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d6346430-970c-4977-8a7c-2631e3032a43", "openfda": {"unii": ["55JG375S6M"], "rxcui": ["1988974", "1988977", "1988980", "1994389", "1994392", "1994395"], "spl_set_id": ["f280bbd8-2af2-444a-bd96-e409337ca6dd"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (58151-245-93)", "package_ndc": "58151-245-93", "marketing_start_date": "20241126"}], "brand_name": "Lyrica CR", "product_id": "58151-245_d6346430-970c-4977-8a7c-2631e3032a43", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "58151-245", "dea_schedule": "CV", "generic_name": "PREGABALIN", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lyrica CR", "active_ingredients": [{"name": "PREGABALIN", "strength": "82.5 mg/1"}], "application_number": "NDA209501", "marketing_category": "NDA", "marketing_start_date": "20241126", "listing_expiration_date": "20261231"}