← FDA Drug Approvals (Drugs@FDA)
PRONESTYL
NDA · New Drug Application · Sponsor: APOTHECON · Approved 1950-06-02
Drug application
- FDA Application #
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
- Authoritative
- Drugs@FDA application overview
- Machine
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