Package 47335-991-02

Brand: glatiramer acetate

Generic: glatiramer acetate
NDC Package

Package Facts

Identity

Package NDC 47335-991-02
Digits Only 4733599102
Product NDC 47335-991
Description

12 BLISTER PACK in 1 CARTON (47335-991-02) / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2025-08-15
Brand glatiramer acetate
Generic glatiramer acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "9153cc14-8516-4cdc-a47e-3b8368f573e5", "openfda": {"unii": ["5M691HL4BO"], "rxcui": ["1487361"], "spl_set_id": ["dfacc3e2-5c91-41de-a377-873276a5cf67"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (47335-991-02)  / 1 SYRINGE in 1 BLISTER PACK / 1 mL in 1 SYRINGE", "package_ndc": "47335-991-02", "marketing_start_date": "20250815"}], "brand_name": "Glatiramer Acetate", "product_id": "47335-991_9153cc14-8516-4cdc-a47e-3b8368f573e5", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "47335-991", "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": "40 mg/mL"}], "application_number": "ANDA206873", "marketing_category": "ANDA", "marketing_start_date": "20250815", "listing_expiration_date": "20261231"}