Micafungin
- Product NDC
- 60505-6119
- 11-digit product format
- 605056119
- Labeler code
- 60505
- Product ID
- 60505-6119_4fb304cc-b35f-4b8e-397b-fddc9a2e524e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Micafungin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Apotex Corp.
- Application
- ANDA208366
- Marketing category
- ANDA
- Marketing start
- 2021-02-12
- Marketing end
- 0000-00-00
- Substance
- MICAFUNGIN
- Active strength
- 10 mg/mL
- Pharmacologic classes
- Echinocandin Antifungal [EPC], Lipopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 60505-6119-5 | 60505611905 | 10 VIAL, SINGLE-USE in 1 CARTON (60505-6119-5) > 5 mL in 1 VIAL, SINGLE-USE | 2021-02-12 | 0000-00-00 | No | No | Current |