Product NDC: | 35356-819 |
Proprietary Name: | PredniSONE |
Non Proprietary Name: | PredniSONE |
Active Ingredient(s): | 5 mg/1 & nbsp; PredniSONE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-819 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA080352 |
Marketing Category: | ANDA |
Start Marketing Date: | 19720421 |
Package NDC: | 35356-819-40 |
Package Description: | 40 TABLET in 1 BOTTLE, PLASTIC (35356-819-40) |
NDC Code | 35356-819-40 |
Proprietary Name | PredniSONE |
Package Description | 40 TABLET in 1 BOTTLE, PLASTIC (35356-819-40) |
Product NDC | 35356-819 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | PredniSONE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19720421 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | PREDNISONE |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |