United States · FDA National Drug Code directory
Glatiramer Acetate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 47335-990_3b31bc9a-3536-4485-ae0d-05acf7c2787d
- Product NDC
- 47335-990
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Glatiramer Acetate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250815
- Source listing expiry
- 20261231
Source-listed ingredients
- GLATIRAMER ACETATE — 20 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 BLISTER PACK in 1 CARTON (47335-990-02) / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE · 47335-990-02
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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