# Valium

NDC: 0140-0004
Generic name: diazepam
Labeler / Manufacturer: Roche Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19631115
Marketing ended: 20270810
FDA application: NDA013263

## Active ingredients

- DIAZEPAM: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0140-0004"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0140-0004
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=554baee5-b171-4452-a50a-41a0946f956c