Carboplatin
- Product NDC
- 50742-445
- 11-digit product format
- 507420445
- Labeler code
- 50742
- Product ID
- 50742-445_a7025e4e-e097-4619-a539-eb1850a4c088
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Carboplatin
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA208487
- Marketing category
- ANDA
- Marketing start
- 2017-05-06
- Marketing end
- 0000-00-00
- Substance
- CARBOPLATIN
- Active strength
- 50 mg/5mL
- Pharmacologic classes
- Platinum-containing Compounds [EXT],Platinum-based Drug [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 |
|---|
| 50742-445-05 | 50742044505 | 1 VIAL, MULTI-DOSE in 1 CARTON (50742-445-05) > 5 mL in 1 VIAL, MULTI-DOSE | 2017-05-06 | 0000-00-00 | No | No | Current |