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Carboplatin
Carboplatin - 61703-339-22 - (Carboplatin)
Drug Information of Carboplatin
| Product NDC: | 61703-339 |
| 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: | 61703-339 |
| Labeler Name: | Hospira Worldwide, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076517 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091217 |
Package Information of Carboplatin
| Package NDC: | 61703-339-22 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-22) > 15 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Carboplatin
| NDC Code | 61703-339-22 |
| Proprietary Name | Carboplatin |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (61703-339-22) > 15 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 61703-339 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carboplatin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091217 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira Worldwide, Inc. |
| Substance Name | CARBOPLATIN |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
