Details for New Drug Application (NDA): 085161
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The generic ingredient in PREDNISONE is prednisone. There are sixteen drug master file entries for this compound. Fifty suppliers are listed for this compound. Additional details are available on the prednisone profile page.
Summary for 085161
Tradename: | PREDNISONE |
Applicant: | Watson Labs |
Ingredient: | prednisone |
Patents: | 0 |
Pharmacology for NDA: 085161
Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
Medical Subject Heading (MeSH) Categories for 085161
Suppliers and Packaging for NDA: 085161
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
PREDNISONE | prednisone | TABLET;ORAL | 085161 | ANDA | Actavis Pharma, Inc. | 0591-5443 | 0591-5443-01 | 100 TABLET in 1 BOTTLE (0591-5443-01) |
PREDNISONE | prednisone | TABLET;ORAL | 085161 | ANDA | Actavis Pharma, Inc. | 0591-5443 | 0591-5443-05 | 500 TABLET in 1 BOTTLE (0591-5443-05) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 20MG | ||||
Approval Date: | Approved Prior to Jan 1, 1982 | TE: | AB | RLD: | No |
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