Paromomycin Sulfate (Sun Pharmaceutical Industries, Inc.)


Welcome to the PulseAid listing for the Paromomycin Sulfate drug offered from Sun Pharmaceutical Industries, Inc.. This Antiprotozoal [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: Sun Pharmaceutical Industries, Inc.
NON-PROPRIETARY NAME: Paromomycin Sulfate
SUBSTANCE NAME: PAROMOMYCIN SULFATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Antiprotozoal [EPC]
ROUTE: ORAL
DOSAGE FORM: CAPSULE
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 1997-06-30
END MARKETING DATE: 0000-00-00


Paromomycin Sulfate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionParomomycin Sulfate from Sun Pharmaceutical Industries, Inc.
LABELER NAME: Sun Pharmaceutical Industries, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 250(mg/1)
START MARKETING DATE: 1997-06-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 57664-175_300906e6-6208-46e4-b8e0-c9613059051a
PRODUCT NDC: 57664-175
APPLICATION NUMBER: ANDA064171

Other PAROMOMYCIN SULFATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Department of State Health Services, Pharmacy BranchParomomycin Sulfate
Heritage Pharmaceuticals Inc.Paromomycin Sulfate
Sun Pharmaceutical Industries, Inc.Paromomycin Sulfate