# Glatiramer Acetate

NDC: 47335-991
Generic name: Glatiramer Acetate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20250815

FDA application: ANDA206873

## Active ingredients

- GLATIRAMER ACETATE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-991"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-991
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dfacc3e2-5c91-41de-a377-873276a5cf67