| Product NDC: | 66780-110 |
| Proprietary Name: | SYMLIN |
| Non Proprietary Name: | pramlintide acetate |
| Active Ingredient(s): | 600 ug/mL & nbsp; pramlintide acetate |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66780-110 |
| Labeler Name: | Amylin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021332 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050316 |
| Package NDC: | 66780-110-01 |
| Package Description: | 5 mL in 1 VIAL, MULTI-DOSE (66780-110-01) |
| NDC Code | 66780-110-01 |
| Proprietary Name | SYMLIN |
| Package Description | 5 mL in 1 VIAL, MULTI-DOSE (66780-110-01) |
| Product NDC | 66780-110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | pramlintide acetate |
| Dosage Form Name | INJECTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20050316 |
| Marketing Category Name | NDA |
| Labeler Name | Amylin Pharmaceuticals, Inc. |
| Substance Name | PRAMLINTIDE ACETATE |
| Strength Number | 600 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Amylin Agonists [MoA],Amylin Analog [EPC] |