# Thiamine Hydrochloride

NDC: 0641-6228
Generic name: Thiamine Hydrochloride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20210212

FDA application: ANDA080575

## 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:"0641-6228"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6228
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63f3631b-ba1e-430c-a30b-dd05b2c00c13