Alprostadil (Teva Parenteral Medicines, Inc.)


Welcome to the PulseAid listing for the Alprostadil drug offered from Teva Parenteral Medicines, Inc.. This Genitourinary Arterial Vasodilation [PE],Prostaglandin Analog [EPC],Prostaglandin E1 Agonist [EPC],Prostaglandin Receptor Agonists [MoA],Prostaglandins [Chemical/Ingredient],Venous Vasodilation [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view the 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: Teva Parenteral Medicines, Inc.
NON-PROPRIETARY NAME: Alprostadil
SUBSTANCE NAME: ALPROSTADIL
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Genitourinary Arterial Vasodilation [PE],Prostaglandin Analog [EPC],Prostaglandin E1 Agonist [EPC],Prostaglandin Receptor Agonists [MoA],Prostaglandins [Chemical/Ingredient],Venous Vasodilation [PE]
ROUTE: INTRAVASCULAR
DOSAGE FORM: INJECTION, SOLUTION, CONCENTRATE
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1999-04-30
END MARKETING DATE: 0000-00-00


Alprostadil HUMAN PRESCRIPTION DRUG Details:

Item DescriptionAlprostadil from Teva Parenteral Medicines, Inc.
LABELER NAME: Teva Parenteral Medicines, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 500(ug/mL)
START MARKETING DATE: 1999-04-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0703-1501_aff8c1fa-b88c-449f-af23-896d74fcdeb2
PRODUCT NDC: 0703-1501
APPLICATION NUMBER: ANDA075196

Other ALPROSTADIL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Actient Pharmaceuticals, LLCEdex
Meda PharmaceuticalsMUSE
Pharmacia and Upjohn Company LLCPROSTIN
Teva Parenteral Medicines, Inc.Alprostadil
U.S. PharmaceuticalsCaverject Impulse