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BYDUREON
BYDUREON - 66780-219-02 - (exenatide)
Drug Information of BYDUREON
| Product NDC: | 66780-219 |
| Proprietary Name: | BYDUREON |
| Non Proprietary Name: | exenatide |
| Active Ingredient(s): | & nbsp; exenatide |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BYDUREON
| Product NDC: | 66780-219 |
| Labeler Name: | Amylin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022200 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120127 |
Package Information of BYDUREON
| Package NDC: | 66780-219-02 |
| Package Description: | 1 TRAY in 1 CARTON (66780-219-02) > 1 KIT in 1 TRAY * .65 mL in 1 VIAL * .65 mL in 1 SYRINGE, GLASS |
NDC Information of BYDUREON
| NDC Code | 66780-219-02 |
| Proprietary Name | BYDUREON |
| Package Description | 1 TRAY in 1 CARTON (66780-219-02) > 1 KIT in 1 TRAY * .65 mL in 1 VIAL * .65 mL in 1 SYRINGE, GLASS |
| Product NDC | 66780-219 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | exenatide |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20120127 |
| Marketing Category Name | NDA |
| Labeler Name | Amylin Pharmaceuticals, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
