Home
>
National Drug Code (NDC)
>
PREDNISONE
PREDNISONE - 24236-248-13 - (PREDNISONE)
Drug Information of PREDNISONE
| Product NDC: | 24236-248 |
| 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: | 24236-248 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088832 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130118 |
Package Information of PREDNISONE
| Package NDC: | 24236-248-13 |
| Package Description: | 16 TABLET in 1 BLISTER PACK (24236-248-13) |
NDC Information of PREDNISONE
| NDC Code | 24236-248-13 |
| Proprietary Name | PREDNISONE |
| Package Description | 16 TABLET in 1 BLISTER PACK (24236-248-13) |
| Product NDC | 24236-248 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREDNISONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130118 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | PREDNISONE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
