Thiamine Hydrochloride
Thiamine HCL 100 mg/mL Injection, USP 2 mL Multi Dose Vial
Approved
Approval ID
7b3587a5-d4ef-4d3d-8430-cbfbaaaf4cb3
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Sep 7, 2010
Manufacturers
FDA
Physicians Total Care, Inc.
DUNS: 194123980
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Thiamine Hydrochloride
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code54868-2489
Application NumberANDA080556
Product Classification
M
Marketing Category
C73584
G
Generic Name
Thiamine Hydrochloride
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateNovember 14, 2011
FDA Product Classification
INGREDIENTS (1)
Thiamine HydrochlorideActive
Quantity: 100 mg in 1 mL
Code: M572600E5P
Classification: ACTIB