Thiamine Hydrochloride Injection, Solution
Product Images NDC 51662-1635

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Thiamine Hydrochloride Injection, Solution (NDC 51662-1635). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

How Supplied (51662 1635 1 How Supplied)

Table presenting the unit of sale, strength, and packaging details for THIAMINE HYDROCHLORIDE injection, solution. It lists a 2 mL multiple dose vial with a strength of 200 mg per 2 mL (100 mg per mL), corresponding to NDC 51662-1635-1.*

FDA Label Image

Serialized Label (51662 1635 1 Serialized Label)

THIAMINE HYDROCHLORIDE injection, solution label with scannable barcode, lot number, and expiration date information. Distributed by HF Acquisition Co LLC, DBA HealthFirst, located in Mukilteo, Washington. Marked RX ONLY.*

FDA Label Image

Structure (51662 1635 1 Structure)

Chemical structure of thiamine hydrochloride showing its molecular formula (C12H17ClN4OS·HCl) and molecular weight (337.27). The diagram depicts the arrangement of atoms including carbon, hydrogen, nitrogen, oxygen, sulfur, and chlorine present in the compound.*

FDA Label Image

Original Mfg Label (Original Mfg Label)

Label for Thiamine HCl Injection, USP 200 mg per 2 mL (100 mg per mL) solution used for intramuscular or intravenous use. The label indicates a 2 mL multiple dose vial. Distributed by Dr. Reddy's Laboratories, Inc., made in India, and includes NDC 43598-050-11 and a lot number code.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.