# TENUATE
> **NDA017669** · New Drug Application · Sponsor: SANOFI AVENTIS US · Approved 1975-03-20
## Drug
- **FDA Application Number:** NDA017669
- **Application type:** New Drug Application
- **Brand name:** TENUATE
- **Generic name:** Diethylpropion Hydrochloride
- **Active ingredients:** DIETHYLPROPION HYDROCHLORIDE
- **Dosage form:** TABLET, EXTENDED RELEASE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** SANOFI AVENTIS US
- **First approval:** 1975-03-20
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=017669)
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