Product NDC: | 49999-153 |
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: | 49999-153 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA011153 |
Marketing Category: | NDA |
Start Marketing Date: | 20120209 |
Package NDC: | 49999-153-21 |
Package Description: | 21 TABLET in 1 DOSE PACK (49999-153-21) |
NDC Code | 49999-153-21 |
Proprietary Name | Methylprednisolone |
Package Description | 21 TABLET in 1 DOSE PACK (49999-153-21) |
Product NDC | 49999-153 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | methylprednisolone |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120209 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | METHYLPREDNISOLONE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |