Home
>
National Drug Code (NDC)
>
PLATINOL
PLATINOL - 0015-3072-97 - (cisplatin)
Drug Information of PLATINOL
| Product NDC: | 0015-3072 |
| Proprietary Name: | PLATINOL |
| Non Proprietary Name: | cisplatin |
| Active Ingredient(s): | 50 mg/50mL & nbsp; cisplatin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PLATINOL
| Product NDC: | 0015-3072 |
| Labeler Name: | E.R. Squibb & Sons, L.L.C. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018057 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050101 |
Package Information of PLATINOL
| Package NDC: | 0015-3072-97 |
| Package Description: | 10 CARTON in 1 CARTON (0015-3072-97) > 1 VIAL in 1 CARTON > 50 mL in 1 VIAL |
NDC Information of PLATINOL
| NDC Code | 0015-3072-97 |
| Proprietary Name | PLATINOL |
| Package Description | 10 CARTON in 1 CARTON (0015-3072-97) > 1 VIAL in 1 CARTON > 50 mL in 1 VIAL |
| Product NDC | 0015-3072 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cisplatin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050101 |
| Marketing Category Name | NDA |
| Labeler Name | E.R. Squibb & Sons, L.L.C. |
| Substance Name | CISPLATIN |
| Strength Number | 50 |
| Strength Unit | mg/50mL |
| Pharmaceutical Classes | Platinum-based Drug [EPC],Platinum-containing Compounds [Chemical/Ingredient] |
