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Glatiramer Acetate

NDC 47335-991 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206873
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsGLATIRAMER ACETATE (40 mg/mL)
Marketing started20250815
Package count1

External sources

Source: openFDA. Public-domain (CC0).