glatiramer acetate
Generic: glatiramer acetate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
glatiramer acetate
Generic Name
glatiramer acetate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
glatiramer acetate 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
47335-990
Product ID
47335-990_3b31bc9a-3536-4485-ae0d-05acf7c2787d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203857
Listing Expiration
2026-12-31
Marketing Start
2025-08-15
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47335990
Hyphenated Format
47335-990
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
glatiramer acetate (source: ndc)
Generic Name
glatiramer acetate (source: ndc)
Application Number
ANDA203857 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 30 BLISTER PACK in 1 CARTON (47335-990-02) / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "3b31bc9a-3536-4485-ae0d-05acf7c2787d", "openfda": {"unii": ["5M691HL4BO"], "rxcui": ["1111641"], "spl_set_id": ["f90cc5f5-56a1-48dc-a4fc-0ae89ef61deb"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (47335-990-02) / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE", "package_ndc": "47335-990-02", "marketing_start_date": "20250815"}], "brand_name": "Glatiramer Acetate", "product_id": "47335-990_3b31bc9a-3536-4485-ae0d-05acf7c2787d", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "47335-990", "generic_name": "Glatiramer Acetate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glatiramer Acetate", "active_ingredients": [{"name": "GLATIRAMER ACETATE", "strength": "20 mg/mL"}], "application_number": "ANDA203857", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}