Mitomycin
- Product NDC
- 67457-520
- 11-digit product format
- 674570520
- Labeler code
- 67457
- Product ID
- 67457-520_cecc31d9-bc8e-4d6f-b46c-4e3b3bea6307
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mitomycin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA203386
- Marketing category
- ANDA
- Marketing start
- 2018-02-28
- Marketing end
- 0000-00-00
- Substance
- MITOMYCIN
- Active strength
- 40 mg/80mL
- Pharmacologic classes
- Alkylating Activity [MoA],Alkylating Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 67457-520-40 | 67457052040 | 1 VIAL in 1 CARTON (67457-520-40) > 80 mL in 1 VIAL | 1 vial | 2018-03-19 | 0000-00-00 | No | No | Current |