# Thiamine Hydrochloride

NDC: 23155-933
Generic name: Thiamine Hydrochloride
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20251115

FDA application: ANDA217181

## Active ingredients

- THIAMINE HYDROCHLORIDE: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-933"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-933
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=764d608a-d821-4447-85e1-6af297abb4c1