# PRONESTYL
> **NDA007335** · New Drug Application · Sponsor: APOTHECON · Approved 1950-06-02
## Drug
- **FDA Application Number:** NDA007335
- **Application type:** New Drug Application
- **Brand name:** PRONESTYL
- **Generic name:** Procainamide Hydrochloride
- **Active ingredients:** PROCAINAMIDE HYDROCHLORIDE
- **Dosage form:** CAPSULE
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** APOTHECON
- **First approval:** 1950-06-02
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=007335)
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