Details for New Drug Application (NDA): 085162
✉ Email this page to a colleague
The generic ingredient in PREDNISONE is prednisone. There are sixteen drug master file entries for this compound. Fifty-one suppliers are listed for this compound. Additional details are available on the prednisone profile page.
Summary for 085162
Tradename: | PREDNISONE |
Applicant: | Watson Labs |
Ingredient: | prednisone |
Patents: | 0 |
Pharmacology for NDA: 085162
Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Medical Subject Heading (MeSH) Categories for 085162
Suppliers and Packaging for NDA: 085162
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PREDNISONE | prednisone | TABLET;ORAL | 085162 | ANDA | Actavis Pharma, Inc. | 0591-5442 | 0591-5442-01 | 100 TABLET in 1 BOTTLE (0591-5442-01) |
PREDNISONE | prednisone | TABLET;ORAL | 085162 | ANDA | Actavis Pharma, Inc. | 0591-5442 | 0591-5442-05 | 500 TABLET in 1 BOTTLE (0591-5442-05) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AB | RLD: | No |
Complete Access Available with Subscription