← FDA Drug Approvals (Drugs@FDA)
PREDNISOLONE SODIUM PHOSPHATE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 1974-01-29
Drug application
- FDA Application #
ANDA080517- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- PREDNISOLONE SODIUM PHOSPHATE
- Generic name
- Prednisolone Sodium Phosphate
- Active ingredients
- PREDNISOLONE SODIUM PHOSPHATE
- Dosage form
- INJECTABLE
- Route
- INJECTION
- Marketing status
- Discontinued
- Sponsor
- WATSON LABS
- First approval
- 1974-01-29
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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