Product NDC: | 16590-149 |
Proprietary Name: | METHYLPREDNISOLONE |
Non Proprietary Name: | METHYLPREDNISOLONE |
Active Ingredient(s): | 4 mg/1 & nbsp; METHYLPREDNISOLONE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-149 |
Labeler Name: | STAT Rx USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040189 |
Marketing Category: | ANDA |
Start Marketing Date: | 19971031 |
Package NDC: | 16590-149-21 |
Package Description: | 21 TABLET in 1 BLISTER PACK (16590-149-21) |
NDC Code | 16590-149-21 |
Proprietary Name | METHYLPREDNISOLONE |
Package Description | 21 TABLET in 1 BLISTER PACK (16590-149-21) |
Product NDC | 16590-149 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | METHYLPREDNISOLONE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19971031 |
Marketing Category Name | ANDA |
Labeler Name | STAT Rx USA LLC |
Substance Name | METHYLPREDNISOLONE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |