Package 55150-273-25

Brand: thiamine hydrochloride

Generic: thiamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-273-25
Digits Only 5515027325
Product NDC 55150-273
Description

25 VIAL, MULTI-DOSE in 1 CARTON (55150-273-25) / 2 mL in 1 VIAL, MULTI-DOSE (55150-273-01)

Marketing

Marketing Status
Marketed Since 2022-04-20
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": "b4f91191-9bfa-41ed-a9ca-221cf44ffc27", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["4985bf3c-abe5-4bbb-9dcc-6de387d36d6b"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (55150-273-25)  / 2 mL in 1 VIAL, MULTI-DOSE (55150-273-01)", "package_ndc": "55150-273-25", "marketing_start_date": "20220420"}], "brand_name": "Thiamine Hydrochloride", "product_id": "55150-273_b4f91191-9bfa-41ed-a9ca-221cf44ffc27", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "55150-273", "generic_name": "Thiamine Hydrochloride", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine Hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "200 mg/2mL"}], "application_number": "ANDA208703", "marketing_category": "ANDA", "marketing_start_date": "20220420", "listing_expiration_date": "20261231"}