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SOMAVERT
SOMAVERT - 0009-5178-01 - (pegvisomant)
Drug Information of SOMAVERT
| Product NDC: | 0009-5178 |
| Proprietary Name: | SOMAVERT |
| Non Proprietary Name: | pegvisomant |
| Active Ingredient(s): | & nbsp; pegvisomant |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SOMAVERT
| Product NDC: | 0009-5178 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021106 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030525 |
Package Information of SOMAVERT
| Package NDC: | 0009-5178-01 |
| Package Description: | 1 KIT in 1 PACKAGE (0009-5178-01) * 1 mL in 1 VIAL, SINGLE-DOSE * 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of SOMAVERT
| NDC Code | 0009-5178-01 |
| Proprietary Name | SOMAVERT |
| Package Description | 1 KIT in 1 PACKAGE (0009-5178-01) * 1 mL in 1 VIAL, SINGLE-DOSE * 1 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0009-5178 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pegvisomant |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20030525 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
