# Diazepam

NDC: 70710-2080
Generic name: Diazepam
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: RECTAL
Marketing started: 20251215

FDA application: ANDA217468

## Active ingredients

- DIAZEPAM: 20 mg/4mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-2080"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-2080
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=652714c7-25c4-4d05-979d-8eee3b6f2f4d