Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 080751
Company: NOVARTIS
Company: NOVARTIS
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
INFLAMASE FORTE | PREDNISOLONE SODIUM PHOSPHATE | EQ 0.9% PHOSPHATE | SOLUTION/DROPS;OPHTHALMIC | Discontinued | None | Yes | No |
INFLAMASE MILD | PREDNISOLONE SODIUM PHOSPHATE | EQ 0.11% PHOSPHATE | SOLUTION/DROPS;OPHTHALMIC | Discontinued | None | Yes | No |
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