Arsenic Trioxide
- Product NDC
- 70860-217
- 11-digit product format
- 708600217
- Labeler code
- 70860
- Product ID
- 70860-217_80ae6afb-9ea9-466e-a9ba-5309224e7efa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- arsenic trioxide
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA209315
- Marketing category
- ANDA
- Marketing start
- 2020-11-30
- Marketing end
- 0000-00-00
- Substance
- ARSENIC TRIOXIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-217-10 | 70860021710 | 1 VIAL in 1 CARTON (70860-217-10) > 10 mL in 1 VIAL | 1 vial | 2020-11-30 | 0000-00-00 | No | No | Current |