Pentoxifylline (Mylan Pharmaceuticals Inc.)
Welcome to the PulseAid listing for the Pentoxifylline drug offered from Mylan Pharmaceuticals Inc.. This Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] 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: | Mylan Pharmaceuticals Inc. |
NON-PROPRIETARY NAME: | Pentoxifylline |
SUBSTANCE NAME: | PENTOXIFYLLINE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Blood Viscosity Reducer [EPC],Hematologic Activity Alteration [PE] |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED, EXTENDED RELEASE |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 1997-07-08 |
END MARKETING DATE: | 0000-00-00 |
Pentoxifylline HUMAN PRESCRIPTION DRUG Details:
Item Description | Pentoxifylline from Mylan Pharmaceuticals Inc. |
LABELER NAME: | Mylan Pharmaceuticals Inc. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 400(mg/1) |
START MARKETING DATE: | 1997-07-08 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0378-0357_bded7f93-7028-43a5-a0bc-822a1a11763a |
PRODUCT NDC: | 0378-0357 |
APPLICATION NUMBER: | ANDA074425 |
Other PENTOXIFYLLINE Pharmaceutical Manufacturers / Labelers: