Lovenox (sanofi-aventis U.S. LLC)


Welcome to the PulseAid listing for the Lovenox drug offered from sanofi-aventis U.S. LLC. This Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [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: enoxaparin sodium
SUBSTANCE NAME: ENOXAPARIN SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Heparin, Low-Molecular-Weight [Chemical/Ingredient],Low Molecular Weight Heparin [EPC]
ROUTE: INTRAVENOUS; SUBCUTANEOUS
DOSAGE FORM: INJECTION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 2008-03-12
END MARKETING DATE: 0000-00-00


Lovenox HUMAN PRESCRIPTION DRUG Details:

Item DescriptionLovenox from sanofi-aventis U.S. LLC
LABELER NAME: sanofi-aventis U.S. LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 40(mg/.4mL)
START MARKETING DATE: 2008-03-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0075-0620_2cb4222b-718d-4e8f-96ce-fc65b9a2738f
PRODUCT NDC: 0075-0620
APPLICATION NUMBER: NDA020164

Other ENOXAPARIN SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Amphastar Pharmaceuticals, Inc.Enoxaparin Sodium
Cardinal HealthEnoxaparin Sodium
Fresenius Kabi USA, LLCEnoxaparin sodium
Physicians Total Care, Inc.Lovenox
Sandoz IncEnoxaparin Sodium
sanofi-aventis U.S. LLCLovenox
Teva Parenteral Medicines, Inc.Enoxaparin Sodium
Watson Pharma, Inc.Enoxaparin Sodium
Winthrop U.S.Enoxaparin sodium