Micafungin
- Product NDC
- 72572-427
- 11-digit product format
- 725720427
- Labeler code
- 72572
- Product ID
- 72572-427_21170a49-4d2a-4992-b104-5d26fd88422a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Micafungin sodium
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA211713
- Marketing category
- ANDA
- Marketing start
- 2021-02-06
- Marketing end
- 0000-00-00
- Substance
- MICAFUNGIN SODIUM
- Active strength
- 100 mg/1
- Pharmacologic classes
- Echinocandin Antifungal [EPC], Lipopeptides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72572-427 | MICAFUNGIN (MICAFUNGIN SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [CIVICA, INC.] | 5 | Legacy NDC | 20231201_b7217896-fb88-44de-afe4-5b1cfef3d4fc.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-427-01 | 72572042701 | 1 VIAL in 1 CARTON (72572-427-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL | 1 vial | 2022-01-08 | 0000-00-00 | No | No | Current |