Class III ยท Low risk
Thiamine HCl Injection
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.
National Drug Code
Is NDC 67457-0196-02 recalled?
Thiamine Hydrochloride · 25 VIAL, MULTI-DOSE in 1 CARTON (67457-196-02) / 2 mL in 1 VIAL, MULTI-DOSE (67457-196-00)
Yes — this exact package was recalled
1 FDA recall names the code 67457-0196-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- thiamine hydrochloride
- Strength
- THIAMINE HYDROCHLORIDE 100 mg/mL
- Form
- Injection, Solution · Intramuscular, Intravenous
- Labeler
- Mylan Institutional LLC
- Type
- Human Prescription Drug
- Product code
- 67457-0196
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 67457-0153 Amiodarone Hydrochloride 2
- 67457-0386 Mycophenolate Mofetil 2
- 67457-0445 Rifampin 2
- 67457-0187 Aloprim 1
- 67457-0197 Tranexamic Acid 1
- 67457-0218 Duraclon 1
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