Soliqua 100/33 (Sanofi-Aventis U.S. LLC)


Welcome to the PulseAid listing for the Soliqua 100/33 drug offered from Sanofi-Aventis U.S. LLC. This Insulin [Chemical/Ingredient],Insulin Analog [EPC],GLP-1 Receptor Agonist [EPC],Glucagon-Like Peptide 1 [Chemical/Ingredient],Glucagon-like Peptide-1 (GLP-1) Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Sanofi-Aventis U.S. LLC
NON-PROPRIETARY NAME: insulin glargine and lixisenatide
SUBSTANCE NAME: INSULIN GLARGINE; LIXISENATIDE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Insulin [Chemical/Ingredient],Insulin Analog [EPC],GLP-1 Receptor Agonist [EPC],Glucagon-Like Peptide 1 [Chemical/Ingredient],Glucagon-like Peptide-1 (GLP-1) Agonists [MoA]
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2016-11-21
END MARKETING DATE: 0000-00-00


Soliqua 100/33 HUMAN PRESCRIPTION DRUG Details:

Item DescriptionSoliqua 100/33 from Sanofi-Aventis U.S. LLC
LABELER NAME: Sanofi-Aventis U.S. LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 100; 33(U/mL; ug/mL)
START MARKETING DATE: 2016-11-21
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0024-5761_e4e75cc9-4d65-46b6-9e7a-d6c433c580e9
PRODUCT NDC: 0024-5761
APPLICATION NUMBER: NDA208673

Other INSULIN GLARGINE; LIXISENATIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Sanofi-Aventis U.S. LLCSoliqua 100/33