Fosaprepitant
- Product NDC
- 68001-675
- 11-digit product format
- 680010675
- Labeler code
- 68001
- Product ID
- 68001-675_40b8d42a-e529-ba9c-e063-6394a90a1b40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fosaprepitant
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- BluePoint Laboratories
- Application
- ANDA209965
- Marketing category
- ANDA
- Marketing start
- 2025-10-15
- Substance
- FOSAPREPITANT DIMEGLUMINE
- Active strength
- 150 mg/5mL
- Pharmacologic classes
- Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Neurokinin 1 Antagonists [MoA], Substance P/Neurokinin-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| D35FM8T64X | FOSAPREPITANT DIMEGLUMINE | 265121-04-8 | FOSAPREPITANT DIMEGLUMINE |
| 6L8OF9XRDC | FOSAPREPITANT | 172673-20-0 | Fosaprepitant |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68001-675-25 | 68001067525 | 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-675-25) / 5 mL in 1 VIAL, SINGLE-DOSE | 2025-10-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Fosaprepitant | BluePoint Laboratories | MSN LABORATORIES PRIVATE LIMITED | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |