NDC 0404-9963
Thiamine Hydrochloride 100 mg per 1 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Mylan Institutional LLC's NDC 67457-196.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Mylan Institutional LLC names for other drugs.
Recalls
- May 3, 2021 · Class III · Mylan Institutional LLC
Labeling: Incorrect or Missing Lot and/or Exp Date: Cartons with the correct lot number 200906 contain vials labeled with the incorrect lot number 200901.
Lots: Lot #: 200906, Exp. Date February 2022
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Thiamine Ion: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 100 mg per 1 mL
- Approval
- ANDA ANDA091623
- On the market since
- Jan 12, 2022
- Package NDCs
0404-9963-02- Official label
- DailyMed (National Library of Medicine), updated Sep 26, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?