# Midazolam

NDC: 70069-818
Generic name: midazolam hydrochloride
Labeler / Manufacturer: SOMERSET THERAPEUTICS, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20231205

FDA application: ANDA090316

## Active ingredients

- MIDAZOLAM HYDROCHLORIDE: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-818"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-818
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=06e4f754-72df-4eb4-aaed-b538524f5277