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Gattex - 68875-0102-1 - (teduglutide)
Drug Information of Gattex
| Product NDC: | 68875-0102 |
| Proprietary Name: | Gattex |
| Non Proprietary Name: | teduglutide |
| Active Ingredient(s): | & nbsp; teduglutide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gattex
| Product NDC: | 68875-0102 |
| Labeler Name: | NPS Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203441 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121221 |
Package Information of Gattex
| Package NDC: | 68875-0102-1 |
| Package Description: | 1 KIT in 1 CARTON (68875-0102-1) * 30 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS * 30 SOLUTION in 1 SYRINGE, PLASTIC |
NDC Information of Gattex
| NDC Code | 68875-0102-1 |
| Proprietary Name | Gattex |
| Package Description | 1 KIT in 1 CARTON (68875-0102-1) * 30 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, GLASS * 30 SOLUTION in 1 SYRINGE, PLASTIC |
| Product NDC | 68875-0102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | teduglutide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20121221 |
| Marketing Category Name | NDA |
| Labeler Name | NPS Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
