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Fluorouracil
Fluorouracil - 68682-004-31 - (Fluorouracil)
Drug Information of Fluorouracil
| Product NDC: | 68682-004 |
| Proprietary Name: | Fluorouracil |
| Non Proprietary Name: | Fluorouracil |
| Active Ingredient(s): | 5 mg/g & nbsp; Fluorouracil |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluorouracil
| Product NDC: | 68682-004 |
| Labeler Name: | Oceanside Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016831 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060901 |
Package Information of Fluorouracil
| Package NDC: | 68682-004-31 |
| Package Description: | 1 TUBE in 1 CARTON (68682-004-31) > 40 g in 1 TUBE |
NDC Information of Fluorouracil
| NDC Code | 68682-004-31 |
| Proprietary Name | Fluorouracil |
| Package Description | 1 TUBE in 1 CARTON (68682-004-31) > 40 g in 1 TUBE |
| Product NDC | 68682-004 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluorouracil |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20060901 |
| Marketing Category Name | NDA |
| Labeler Name | Oceanside Pharmaceuticals |
| Substance Name | FLUOROURACIL |
| Strength Number | 5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
