Package 67457-196-02

Brand: thiamine hydrochloride

Generic: thiamine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67457-196-02
Digits Only 6745719602
Product NDC 67457-196
Description

25 VIAL, MULTI-DOSE in 1 CARTON (67457-196-02) / 2 mL in 1 VIAL, MULTI-DOSE (67457-196-00)

Marketing

Marketing Status
Marketed Since 2013-06-04
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": "cbc5513d-4341-455c-b435-53dd5624efaa", "openfda": {"unii": ["M572600E5P"], "rxcui": ["313324"], "spl_set_id": ["12986d0e-b8bf-4338-9d85-07f973b35439"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (67457-196-02)  / 2 mL in 1 VIAL, MULTI-DOSE (67457-196-00)", "package_ndc": "67457-196-02", "marketing_start_date": "20130604"}], "brand_name": "Thiamine Hydrochloride", "product_id": "67457-196_cbc5513d-4341-455c-b435-53dd5624efaa", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "67457-196", "generic_name": "thiamine hydrochloride", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Thiamine Hydrochloride", "active_ingredients": [{"name": "THIAMINE HYDROCHLORIDE", "strength": "100 mg/mL"}], "application_number": "ANDA091623", "marketing_category": "ANDA", "marketing_start_date": "20130604", "listing_expiration_date": "20261231"}