Package 0378-6961-12

Brand: glatiramer acetate

Generic: glatiramer
NDC Package

Package Facts

Identity

Package NDC 0378-6961-12
Digits Only 0378696112
Product NDC 0378-6961
Description

12 BLISTER PACK in 1 CARTON (0378-6961-12) / 1 SYRINGE in 1 BLISTER PACK (0378-6961-32) / 1 mL in 1 SYRINGE

Marketing

Marketing Status
Marketed Since 2017-10-04
Brand glatiramer acetate
Generic glatiramer
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "f5070abd-2219-47fa-8ff2-c0b147ea3eb7", "openfda": {"unii": ["5M691HL4BO"], "rxcui": ["1487361"], "spl_set_id": ["456a34c7-8511-4000-99a7-ad8f8de6d35e"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 CARTON (0378-6961-12)  / 1 SYRINGE in 1 BLISTER PACK (0378-6961-32)  / 1 mL in 1 SYRINGE", "package_ndc": "0378-6961-12", "marketing_start_date": "20171004"}], "brand_name": "Glatiramer Acetate", "product_id": "0378-6961_f5070abd-2219-47fa-8ff2-c0b147ea3eb7", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0378-6961", "generic_name": "Glatiramer", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Glatiramer Acetate", "active_ingredients": [{"name": "GLATIRAMER ACETATE", "strength": "40 mg/mL"}], "application_number": "ANDA206936", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20261231"}