Product NDC: | 54868-5384 |
Proprietary Name: | BYETTA |
Non Proprietary Name: | exenatide |
Active Ingredient(s): | 250 ug/mL & nbsp; exenatide |
Administration Route(s): | SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5384 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021773 |
Marketing Category: | NDA |
Start Marketing Date: | 20050809 |
Package NDC: | 54868-5384-0 |
Package Description: | 1.2 mL in 1 CARTRIDGE (54868-5384-0) |
NDC Code | 54868-5384-0 |
Proprietary Name | BYETTA |
Package Description | 1.2 mL in 1 CARTRIDGE (54868-5384-0) |
Product NDC | 54868-5384 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | exenatide |
Dosage Form Name | INJECTION |
Route Name | SUBCUTANEOUS |
Start Marketing Date | 20050809 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | EXENATIDE |
Strength Number | 250 |
Strength Unit | ug/mL |
Pharmaceutical Classes | GLP-1 Receptor Agonist [EPC],Glucagon-Like Peptide 1 [Chemical/Ingredient],Glucagon-like Peptide-1 (GLP-1) Agonists [MoA] |