CLOFARABINE
- Product NDC
- 50742-512
- 11-digit product format
- 507420512
- Labeler code
- 50742
- Product ID
- 50742-512_b3c9f25d-eccf-4410-a48c-6caa5f315f73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- clofarabine
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA210270
- Marketing category
- ANDA
- Marketing start
- 2018-09-27
- Marketing end
- 0000-00-00
- Substance
- CLOFARABINE
- Active strength
- 1 mg/mL
- 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 |
|---|
| 50742-512-20 | 50742051220 | 1 VIAL, SINGLE-DOSE in 1 CARTON (50742-512-20) > 20 mL in 1 VIAL, SINGLE-DOSE | 2018-09-27 | 0000-00-00 | No | No | Current |