← FDA Drug Approvals (Drugs@FDA)
ISUPREL
NDA · New Drug Application · Sponsor: SANOFI AVENTIS US · Approved 1948-02-19
Drug application
- FDA Application #
NDA006328- Application type
- New Drug Application
- Brand name
- ISUPREL
- Generic name
- Isoproterenol Hydrochloride
- Active ingredients
- ISOPROTERENOL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- RECTAL, SUBLINGUAL
- Marketing status
- Discontinued
- Sponsor
- SANOFI AVENTIS US
- First approval
- 1948-02-19
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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