Glatiramer Acetate (Mylan Pharmaceuticals Inc.)


Welcome to the PulseAid listing for the Glatiramer Acetate drug offered from Mylan Pharmaceuticals Inc.. This 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: glatiramer acetate
SUBSTANCE NAME: GLATIRAMER ACETATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: SUBCUTANEOUS
DOSAGE FORM: INJECTION, SOLUTION
MARKETING CATEGORY NAME: ANDA
START MARKETING DATE: 2017-10-04
END MARKETING DATE: 0000-00-00


Glatiramer Acetate HUMAN PRESCRIPTION DRUG Details:

Item DescriptionGlatiramer Acetate from Mylan Pharmaceuticals Inc.
LABELER NAME: Mylan Pharmaceuticals Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 20(mg/mL)
START MARKETING DATE: 2017-10-04
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0378-6960_f38b5606-d2d7-44ec-912f-46882aa2fa7b
PRODUCT NDC: 0378-6960
APPLICATION NUMBER: ANDA091646

Other GLATIRAMER ACETATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Mylan Pharmaceuticals Inc.Glatiramer Acetate
Sandoz IncGlatopa
Teva Neuroscience, Inc.Copaxone