Decitabine
- Product NDC
- 64679-067
- 11-digit product format
- 646790067
- Labeler code
- 64679
- Product ID
- 64679-067_0203d7b9-3d86-4a8c-b7e2-11d31d803c71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- decitabine
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA209056
- Marketing category
- ANDA
- Marketing start
- 2020-12-14
- 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
- 2021-12-31
- 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 |
|---|
| 64679-067-02 | 64679006702 | 1 VIAL, SINGLE-USE in 1 CARTON (64679-067-02) > 20 mL in 1 VIAL, SINGLE-USE (64679-067-01) | 2020-12-14 | 0000-00-00 | No | No | Current |