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PredniSONE
PredniSONE - 24236-217-55 - (PredniSONE)
Drug Information of PredniSONE
| Product NDC: | 24236-217 |
| Proprietary Name: | PredniSONE |
| Non Proprietary Name: | PredniSONE |
| Active Ingredient(s): | 10 mg/1 & nbsp; PredniSONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PredniSONE
| Product NDC: | 24236-217 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087800 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130213 |
Package Information of PredniSONE
| Package NDC: | 24236-217-55 |
| Package Description: | 42 TABLET in 1 VIAL (24236-217-55) |
NDC Information of PredniSONE
| NDC Code | 24236-217-55 |
| Proprietary Name | PredniSONE |
| Package Description | 42 TABLET in 1 VIAL (24236-217-55) |
| Product NDC | 24236-217 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PredniSONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130213 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | PREDNISONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
