Pentostatin
- Product NDC
- 67457-288
- 11-digit product format
- 674570288
- Labeler code
- 67457
- Product ID
- 67457-288_9abd3876-d57c-4610-879c-2f30b06e7af1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Pentostatin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA203554
- Marketing category
- ANDA
- Marketing start
- 2014-09-19
- Marketing end
- 0000-00-00
- Substance
- PENTOSTATIN
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC]
- 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 |
|---|
| 67457-288-05 | 67457028805 | 1 VIAL, SINGLE-DOSE in 1 CARTON (67457-288-05) > 5 mL in 1 VIAL, SINGLE-DOSE | 2014-09-19 | 0000-00-00 | No | No | Current |