← FDA Drug Approvals (Drugs@FDA)
SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 1981-11-24
Drug application
- FDA Application #
ANDA087398- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- SPIRONOLACTONE AND HYDROCHLOROTHIAZIDE
- Generic name
- Hydrochlorothiazide
- Active ingredients
- HYDROCHLOROTHIAZIDE; SPIRONOLACTONE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- WATSON LABS
- First approval
- 1981-11-24
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown