Home
>
National Drug Code (NDC)
>
Prednisone
Prednisone - 53808-0543-1 - (PREDNISONE)
Drug Information of Prednisone
| Product NDC: | 53808-0543 |
| Proprietary Name: | Prednisone |
| Non Proprietary Name: | PREDNISONE |
| Active Ingredient(s): | 20 mg/1 & nbsp; PREDNISONE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prednisone
| Product NDC: | 53808-0543 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040392 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of Prednisone
| Package NDC: | 53808-0543-1 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (53808-0543-1) |
NDC Information of Prednisone
| NDC Code | 53808-0543-1 |
| Proprietary Name | Prednisone |
| Package Description | 30 TABLET in 1 BLISTER PACK (53808-0543-1) |
| Product NDC | 53808-0543 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREDNISONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | PREDNISONE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
