Details for New Drug Application (NDA): 075988
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The generic ingredient in PREDNISOLONE SODIUM PHOSPHATE is prednisolone sodium phosphate. There are eighty-eight drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the prednisolone sodium phosphate profile page.
Summary for 075988
Tradename: | PREDNISOLONE SODIUM PHOSPHATE |
Applicant: | Chartwell Rx |
Ingredient: | prednisolone sodium phosphate |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 075988
Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Suppliers and Packaging for NDA: 075988
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PREDNISOLONE SODIUM PHOSPHATE | prednisolone sodium phosphate | SOLUTION;ORAL | 075988 | ANDA | Pharmaceutical Associates, Inc. | 0121-0902 | 0121-0902-04 | 120 mL in 1 BOTTLE (0121-0902-04) |
PREDNISOLONE SODIUM PHOSPHATE | prednisolone sodium phosphate | SOLUTION;ORAL | 075988 | ANDA | Chartwell RX, LLC. | 62135-330 | 62135-330-41 | 120 mL in 1 BOTTLE (62135-330-41) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | SOLUTION;ORAL | Strength | EQ 5MG BASE/5ML | ||||
Approval Date: | May 25, 2004 | TE: | AA | RLD: | No |
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