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Carboplatin
Carboplatin - 63323-172-45 - (Carboplatin)
Drug Information of Carboplatin
| Product NDC: | 63323-172 |
| Proprietary Name: | Carboplatin |
| Non Proprietary Name: | Carboplatin |
| Active Ingredient(s): | 10 mg/mL & nbsp; Carboplatin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carboplatin
| Product NDC: | 63323-172 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077432 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090915 |
Package Information of Carboplatin
| Package NDC: | 63323-172-45 |
| Package Description: | 1 VIAL in 1 BOX (63323-172-45) > 45 mL in 1 VIAL |
NDC Information of Carboplatin
| NDC Code | 63323-172-45 |
| Proprietary Name | Carboplatin |
| Package Description | 1 VIAL in 1 BOX (63323-172-45) > 45 mL in 1 VIAL |
| Product NDC | 63323-172 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carboplatin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090915 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CARBOPLATIN |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
