# Midazolam

NDC: 70069-816
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: ANDA090315

## Active ingredients

- MIDAZOLAM HYDROCHLORIDE: 2 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-816"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-816
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74666098-1ca8-4c06-8fc4-5de870b1b514