BYETTA - 66780-212-01 - (exenatide)

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Drug Information of BYETTA

Product NDC: 66780-212
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)

Labeler Information of BYETTA

Product NDC: 66780-212
Labeler Name: Amylin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021773
Marketing Category: NDA
Start Marketing Date: 20050428

Package Information of BYETTA

Package NDC: 66780-212-01
Package Description: 2.4 mL in 1 CARTRIDGE (66780-212-01)

NDC Information of BYETTA

NDC Code 66780-212-01
Proprietary Name BYETTA
Package Description 2.4 mL in 1 CARTRIDGE (66780-212-01)
Product NDC 66780-212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name exenatide
Dosage Form Name INJECTION
Route Name SUBCUTANEOUS
Start Marketing Date 20050428
Marketing Category Name NDA
Labeler Name Amylin Pharmaceuticals, 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]

Complete Information of BYETTA


General Information