# Thiamine Hydrochloride

NDC: 31722-363
Generic name: Thiamine Hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20241106

FDA application: ANDA218471

## Active ingredients

- THIAMINE HYDROCHLORIDE: 100 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-363"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-363
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d402a31-3240-42a0-bd34-8fccd6a792d3