Decitabine
- Product NDC
- 16714-749
- 11-digit product format
- 167140749
- Labeler code
- 16714
- Product ID
- 16714-749_e2ec1896-aab7-4f58-8911-60cb5a402ff4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Decitabine
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- NorthStar RxLLC
- Application
- ANDA208601
- Marketing category
- ANDA
- Marketing start
- 2017-11-20
- Marketing end
- 0000-00-00
- Substance
- DECITABINE
- Active strength
- 50 mg/20mL
- Pharmacologic classes
- Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [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 |
|---|
| 16714-749-01 | 16714074901 | 1 VIAL in 1 CARTON (16714-749-01) > 20 mL in 1 VIAL | 1 vial | 2017-11-20 | 0000-00-00 | No | No | Current |