# Midazolam

NDC: 70518-4328
Generic name: midazolam hydrochloride
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20250414

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:"70518-4328"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4328
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9305142-417d-4d8c-9a23-f9a1b6771cac