Prednisolone sodium phosphate; sulfacetamide sodium - Generic Drug Details
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What are the generic drug sources for prednisolone sodium phosphate; sulfacetamide sodium and what is the scope of patent protection?
Prednisolone sodium phosphate; sulfacetamide sodium
is the generic ingredient in three branded drugs marketed by Bausch And Lomb, Sandoz, Epic Pharma Llc, and Novartis, and is included in four NDAs. Additional information is available in the individual branded drug profile pages.Three suppliers are listed for this compound.
Summary for prednisolone sodium phosphate; sulfacetamide sodium
US Patents: | 0 |
Tradenames: | 3 |
Applicants: | 4 |
NDAs: | 4 |
Finished Product Suppliers / Packagers: | 3 |
DailyMed Link: | prednisolone sodium phosphate; sulfacetamide sodium at DailyMed |
Pharmacology for prednisolone sodium phosphate; sulfacetamide sodium
Drug Class | Corticosteroid Sulfonamide Antibacterial |
Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
US Patents and Regulatory Information for prednisolone sodium phosphate; sulfacetamide sodium
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Bausch And Lomb | SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE | prednisolone sodium phosphate; sulfacetamide sodium | SOLUTION/DROPS;OPHTHALMIC | 074449-001 | Dec 29, 1995 | RX | No | Yes | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Epic Pharma Llc | SULSTER | prednisolone sodium phosphate; sulfacetamide sodium | SOLUTION/DROPS;OPHTHALMIC | 074511-001 | Jul 30, 1996 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Novartis | VASOCIDIN | prednisolone sodium phosphate; sulfacetamide sodium | SOLUTION/DROPS;OPHTHALMIC | 018988-001 | Aug 26, 1988 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
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