Afrezza (Sanofi-Aventis U.S. LLC)


Welcome to the PulseAid listing for the Afrezza drug offered from Sanofi-Aventis U.S. LLC. This Insulin [Chemical/Ingredient],Insulin [EPC] 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 Human
SUBSTANCE NAME: INSULIN HUMAN
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Insulin [Chemical/Ingredient],Insulin [EPC]
ROUTE: RESPIRATORY (INHALATION)
DOSAGE FORM: POWDER, METERED
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2014-07-11
END MARKETING DATE: 0000-00-00


Afrezza HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAfrezza from Sanofi-Aventis U.S. LLC
LABELER NAME: Sanofi-Aventis U.S. LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 4(1-Jan)
START MARKETING DATE: 2014-07-11
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0024-5874_596bfcee-8076-4cb8-a100-317f23c3c570
PRODUCT NDC: 0024-5874
APPLICATION NUMBER: NDA022472

Other INSULIN HUMAN Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
A-S Medication SolutionsHumulin
Eli Lilly and CompanyHumulin
Mannkind CorporationAfrezza
Novo NordiskNovolin
Physicians Total Care, Inc.Humalog 70/30
Sanofi-Aventis U.S. LLCAfrezza
TYA PharmaceuticalsNovolin