# Diazepam

NDC: 70518-0014
Generic name: Diazepam
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20161130

FDA application: ANDA071322

## Active ingredients

- DIAZEPAM: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-0014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-0014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d7a4b3c7-7021-4764-8c21-49e4bc6f6058