fosaprepitant dimeglumine
- Product NDC
- 0781-3484
- 11-digit product format
- 007813484
- Labeler code
- 0781
- Product ID
- 0781-3484_e8055dfe-f5cd-4784-84e6-2d105b0d4c91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fosaprepitant dimeglumine
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sandoz Inc
- Application
- ANDA203939
- Marketing category
- ANDA
- Marketing start
- 2022-02-16
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0781-3484-75 | 00781348475 | 1 VIAL, SINGLE-USE in 1 CARTON (0781-3484-75) > 5 mL in 1 VIAL, SINGLE-USE | 2022-02-16 | 0000-00-00 | No | No | Current |