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Saizen
Saizen - 44087-1088-1 - (somatropin)
Drug Information of Saizen
| Product NDC: | 44087-1088 |
| Proprietary Name: | Saizen |
| Non Proprietary Name: | somatropin |
| Active Ingredient(s): | & nbsp; somatropin |
| Administration Route(s): | INTRAMUSCULAR; SUBCUTANEOUS |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Saizen
| Product NDC: | 44087-1088 |
| Labeler Name: | EMD Serono, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019764 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000829 |
Package Information of Saizen
| Package NDC: | 44087-1088-1 |
| Package Description: | 1 KIT in 1 CARTON * 3 mL in 1 VIAL, GLASS * 3.5 mL in 1 VIAL, GLASS |
NDC Information of Saizen
| NDC Code | 44087-1088-1 |
| Proprietary Name | Saizen |
| Package Description | 1 KIT in 1 CARTON * 3 mL in 1 VIAL, GLASS * 3.5 mL in 1 VIAL, GLASS |
| Product NDC | 44087-1088 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | somatropin |
| Dosage Form Name | KIT |
| Route Name | INTRAMUSCULAR; SUBCUTANEOUS |
| Start Marketing Date | 20000829 |
| Marketing Category Name | NDA |
| Labeler Name | EMD Serono, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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