Package 25021-500-02
Brand: thiamine hydrochloride
Generic: thiamine hydrochloridePackage Facts
Identity
Package NDC
25021-500-02
Digits Only
2502150002
Product NDC
25021-500
Description
25 VIAL in 1 CARTON (25021-500-02) / 2 mL in 1 VIAL
Marketing
Marketing Status
Brand
thiamine hydrochloride
Generic
thiamine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "644d12b5-9a05-47dc-9e1c-d8f6fe9bbec2", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["5982cf83-01d6-4acb-8373-339079b8a76e"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (25021-500-02) / 2 mL in 1 VIAL", "package_ndc": "25021-500-02", "marketing_start_date": "20210120"}], "brand_name": "thiamine hydrochloride", "product_id": "25021-500_644d12b5-9a05-47dc-9e1c-d8f6fe9bbec2", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "25021-500", "generic_name": "thiamine hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "thiamine hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA206106", "marketing_category": "ANDA", "marketing_start_date": "20210120", "listing_expiration_date": "20261231"}