# Midazolam in Sodium Chloride

NDC: 25021-688
Generic name: Midazolam Hydrochloride
Labeler / Manufacturer: Sagent Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250415

FDA application: ANDA218993

## Active ingredients

- MIDAZOLAM HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"25021-688"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=25021-688
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c546cfd4-4f2b-4b94-aa47-995595f1a146