Fosaprepitant
- Product NDC
- 70860-782
- 11-digit product format
- 708600782
- Labeler code
- 70860
- Product ID
- 70860-782_9661d547-d47a-4caf-8da1-a049797e165a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fosaprepitant dimeglumine
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA212309
- Marketing category
- ANDA
- Marketing start
- 2020-11-30
- Marketing end
- 0000-00-00
- Substance
- FOSAPREPITANT DIMEGLUMINE
- Active strength
- 150 mg/5mL
- Pharmacologic classes
- Neurokinin 1 Antagonists [MoA],Substance P/Neurokinin-1 Receptor Antagonist [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C9 Inducers [MoA],Cytochrome P450 3A4 Inducers [MoA]
- 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 |
|---|
| 70860-782-10 | 70860078210 | 1 VIAL in 1 CARTON (70860-782-10) > 5 mL in 1 VIAL | 1 vial | 2020-11-30 | 0000-00-00 | No | No | Current |