ethacrynic sodium (Oceanside Pharmaceuticals)


Welcome to the PulseAid listing for the ethacrynic sodium drug offered from Oceanside Pharmaceuticals. This Increased Diuresis at Loop of Henle [PE],Loop Diuretic [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: Oceanside Pharmaceuticals
NON-PROPRIETARY NAME: ethacrynic sodium
SUBSTANCE NAME: ETHACRYNATE SODIUM
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]
ROUTE: INTRAVENOUS
DOSAGE FORM: POWDER, FOR SOLUTION
MARKETING CATEGORY NAME: NDA AUTHORIZED GENERIC
START MARKETING DATE: 1967-01-10
END MARKETING DATE: 0000-00-00


ethacrynic sodium HUMAN PRESCRIPTION DRUG Details:

Item Descriptionethacrynic sodium from Oceanside Pharmaceuticals
LABELER NAME: Oceanside Pharmaceuticals
DEA SCHEDULE:
ACTIVE STRENGTH: 50(mg/50mL)
START MARKETING DATE: 1967-01-10
END MARKETING DATE: 0000-00-00
PRODUCT ID: 68682-012_e3a435a1-2edd-4bc8-88ca-9c58203f3897
PRODUCT NDC: 68682-012
APPLICATION NUMBER: NDA016093

Other ETHACRYNATE SODIUM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Aton Pharma, Inc.Sodium Edecrin
Mylan Institutional LLCEthacrynic Sodium
Oceanside Pharmaceuticalsethacrynic sodium
Par Pharmaceutical, Inc.ETHACRYNATE SODIUM