Product NDC: | 58468-0030 |
Proprietary Name: | Thyrogen |
Non Proprietary Name: | THYROTROPIN ALFA |
Active Ingredient(s): | .9 mg/mL & nbsp; THYROTROPIN ALFA |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58468-0030 |
Labeler Name: | Genzyme Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020898 |
Marketing Category: | NDA |
Start Marketing Date: | 19981130 |
Package NDC: | 58468-0030-2 |
Package Description: | 2 VIAL in 1 KIT (58468-0030-2) > 1 mL in 1 VIAL |
NDC Code | 58468-0030-2 |
Proprietary Name | Thyrogen |
Package Description | 2 VIAL in 1 KIT (58468-0030-2) > 1 mL in 1 VIAL |
Product NDC | 58468-0030 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | THYROTROPIN ALFA |
Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19981130 |
Marketing Category Name | NDA |
Labeler Name | Genzyme Corporation |
Substance Name | THYROTROPIN ALFA |
Strength Number | .9 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Thyroid Stimulating Hormone [EPC],Thyrotropin [Chemical/Ingredient] |