Orange Book product
PREDNISOLONE SODIUM PHOSPHATE EQ 0.11% PHOSPHATE
Orange Book ANDA 081043 · ALCON PHARMACEUTICALS LTD · Discontinued
Key facts
| Proprietary name | PREDNISOLONE SODIUM PHOSPHATE |
|---|---|
| Active ingredients | PREDNISOLONE SODIUM PHOSPHATE |
| Strength | EQ 0.11% PHOSPHATE |
| Dosage form | SOLUTION/DROPS |
| Route | OPHTHALMIC |
| Application | ANDA081043 |
| Applicant holder | ALCON PHARMACEUTICALS LTD |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Oct 24, 1991 |
At a glance
- None Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.