# Diazepam

NDC: 70518-2358
Generic name: DIAZEPAM
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20191010

FDA application: ANDA210363

## Active ingredients

- DIAZEPAM: 10 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2358"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2358
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c57af2a2-aa9a-4dac-a200-e0d845005d05