FLUOROURACIL
- Product NDC
- 50742-482
- 11-digit product format
- 507420482
- Labeler code
- 50742
- Product ID
- 50742-482_ca170741-54f2-4647-9d1f-401127c61df3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluorouracil
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA209271
- Marketing category
- ANDA
- Marketing start
- 2019-12-21
- Marketing end
- 0000-00-00
- Substance
- FLUOROURACIL
- Active strength
- 3 g/50mL
- Pharmacologic classes
- Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-482-50 | 50742048250 | 1 VIAL in 1 CARTON (50742-482-50) > 50 mL in 1 VIAL | 1 vial | 2019-12-21 | 0000-00-00 | No | No | Current |