Package 0093-8231-28
Brand: sunitinib malate
Generic: sunitinib malatePackage Facts
Identity
Package NDC
0093-8231-28
Digits Only
0093823128
Product NDC
0093-8231
Description
28 CAPSULE in 1 BOTTLE (0093-8231-28)
Marketing
Marketing Status
Brand
sunitinib malate
Generic
sunitinib malate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "20ff6da6-32c4-421d-b7b0-604a502bfcb5", "openfda": {"unii": ["LVX8N1UT73"], "rxcui": ["616279", "616285", "616289", "1541890"], "spl_set_id": ["a9479e5f-914f-46ca-95c1-327c66457e47"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "28 CAPSULE in 1 BOTTLE (0093-8231-28)", "package_ndc": "0093-8231-28", "marketing_start_date": "20211222"}], "brand_name": "Sunitinib Malate", "product_id": "0093-8231_20ff6da6-32c4-421d-b7b0-604a502bfcb5", "dosage_form": "CAPSULE", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "0093-8231", "generic_name": "Sunitinib Malate", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sunitinib Malate", "active_ingredients": [{"name": "SUNITINIB MALATE", "strength": "50 mg/1"}], "application_number": "ANDA213803", "marketing_category": "ANDA", "marketing_start_date": "20211222", "listing_expiration_date": "20261231"}