ARSENIC TRIOXIDE
- Product NDC
- 50742-525
- 11-digit product format
- 507420525
- Labeler code
- 50742
- Product ID
- 50742-525_475ea9f0-1248-48d0-8333-98bb46bce874
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- arsenic trioxide
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA209315
- Marketing category
- ANDA
- Marketing start
- 2021-01-27
- Marketing end
- 0000-00-00
- Substance
- ARSENIC TRIOXIDE
- Active strength
- 2 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50742-525-07 | 50742052507 | 10 VIAL, SINGLE-DOSE in 1 CARTON (50742-525-07) > 6 mL in 1 VIAL, SINGLE-DOSE (50742-525-06) | 2021-01-27 | 0000-00-00 | No | No | Current |