Enoxaparin Sodium (Sandoz Inc)


Welcome to the PulseAid listing for the Enoxaparin Sodium drug offered from Sandoz Inc. 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: Sandoz Inc
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: ANDA
START MARKETING DATE: 2012-04-23
END MARKETING DATE: 2017-11-30


Enoxaparin Sodium HUMAN PRESCRIPTION DRUG Details:

Item DescriptionEnoxaparin Sodium from Sandoz Inc
LABELER NAME: Sandoz Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 100(mg/mL)
START MARKETING DATE: 2012-04-23
END MARKETING DATE: 2017-11-30
PRODUCT ID: 0781-3122_163bc9b9-b926-4437-8a0b-9d17fd30340d
PRODUCT NDC: 0781-3122
APPLICATION NUMBER: ANDA078660

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