Package 51662-1635-1

Brand: thiamine hydrochloride injection, solution

Generic: thiamine hydrochloride injection, solution
NDC Package

Package Facts

Identity

Package NDC 51662-1635-1
Digits Only 5166216351
Product NDC 51662-1635
Description

2 mL in 1 VIAL, MULTI-DOSE (51662-1635-1)

Marketing

Marketing Status
Marketed Since 2023-09-26
Brand thiamine hydrochloride injection, solution
Generic thiamine hydrochloride injection, solution
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3972cf2f-88ce-e507-e063-6394a90a8da5", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["06446e9a-0e85-0623-e063-6294a90ac403"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL, MULTI-DOSE (51662-1635-1)", "package_ndc": "51662-1635-1", "marketing_start_date": "20230926"}], "brand_name": "THIAMINE HYDROCHLORIDE injection, solution", "product_id": "51662-1635_3972cf2f-88ce-e507-e063-6394a90a8da5", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "51662-1635", "generic_name": "THIAMINE HYDROCHLORIDE injection, solution", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "THIAMINE HYDROCHLORIDE injection, solution", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA080571", "marketing_category": "ANDA", "marketing_start_date": "20230926", "listing_expiration_date": "20261231"}