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FLUOROURACIL
FLUOROURACIL - 21695-829-40 - (fluorouracil)
Drug Information of FLUOROURACIL
| Product NDC: | 21695-829 |
| 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) |
Labeler Information of FLUOROURACIL
| Product NDC: | 21695-829 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077524 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080411 |
Package Information of FLUOROURACIL
| Package NDC: | 21695-829-40 |
| Package Description: | 40 g in 1 TUBE (21695-829-40) |
NDC Information of FLUOROURACIL
| NDC Code | 21695-829-40 |
| Proprietary Name | FLUOROURACIL |
| Package Description | 40 g in 1 TUBE (21695-829-40) |
| Product NDC | 21695-829 |
| 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 | Rebel Distributors Corp |
| Substance Name | FLUOROURACIL |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
