Product NDC: | 66530-249 |
Proprietary Name: | FLUOROURACIL |
Non Proprietary Name: | fluorouracil |
Active Ingredient(s): | 50 mg/g & nbsp; fluorouracil |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66530-249 |
Labeler Name: | Spear Dermatology Products |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077524 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080411 |
Package NDC: | 66530-249-40 |
Package Description: | 40 g in 1 TUBE (66530-249-40) |
NDC Code | 66530-249-40 |
Proprietary Name | FLUOROURACIL |
Package Description | 40 g in 1 TUBE (66530-249-40) |
Product NDC | 66530-249 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluorouracil |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20080411 |
Marketing Category Name | ANDA |
Labeler Name | Spear Dermatology Products |
Substance Name | FLUOROURACIL |
Strength Number | 50 |
Strength Unit | mg/g |
Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |