Package 70518-4230-0

Brand: thiamine hydrochloride

Generic: thiamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4230-0
Digits Only 7051842300
Product NDC 70518-4230
Product ID 70518-4230_4005d19e-7cd8-f2db-e063-6394a90a9e7e
Description

25 VIAL in 1 CARTON (70518-4230-0) / 2 mL in 1 VIAL (70518-4230-1)

Marketing

Marketing Status
Marketed Since 2024-11-13
Brand thiamine hydrochloride
Generic thiamine hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4005d19e-7cd8-f2db-e063-6394a90a9e7e", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["0f38c4ba-cebf-49f4-b0a6-8a5d3ebf618c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70518-4230-0)  / 2 mL in 1 VIAL (70518-4230-1)", "package_ndc": "70518-4230-0", "marketing_start_date": "20241113"}], "brand_name": "Thiamine Hydrochloride", "product_id": "70518-4230_4005d19e-7cd8-f2db-e063-6394a90a9e7e", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "70518-4230", "generic_name": "Thiamine Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine Hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA080575", "marketing_category": "ANDA", "marketing_start_date": "20241113", "listing_expiration_date": "20261231"}