← FDA Drug Approvals (Drugs@FDA)
METHYLDOPA AND HYDROCHLOROTHIAZIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 1989-01-19
Drug application
- FDA Application #
ANDA070959- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- METHYLDOPA AND HYDROCHLOROTHIAZIDE
- Generic name
- Hydrochlorothiazide
- Active ingredients
- HYDROCHLOROTHIAZIDE; METHYLDOPA
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- WATSON LABS
- First approval
- 1989-01-19
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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