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Fluorouracil
Fluorouracil - 51672-4062-1 - (Fluorouracil)
Drug Information of Fluorouracil
| Product NDC: | 51672-4062 |
| Proprietary Name: | Fluorouracil |
| Non Proprietary Name: | Fluorouracil |
| Active Ingredient(s): | 20 mg/mL & nbsp; Fluorouracil |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluorouracil
| Product NDC: | 51672-4062 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076526 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031105 |
Package Information of Fluorouracil
| Package NDC: | 51672-4062-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (51672-4062-1) > 10 mL in 1 BOTTLE |
NDC Information of Fluorouracil
| NDC Code | 51672-4062-1 |
| Proprietary Name | Fluorouracil |
| Package Description | 1 BOTTLE in 1 CARTON (51672-4062-1) > 10 mL in 1 BOTTLE |
| Product NDC | 51672-4062 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluorouracil |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20031105 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | FLUOROURACIL |
| Strength Number | 20 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
