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Prednisone
Prednisone - 49349-997-02 - (PREDNISONE)
Drug Information of Prednisone
| Product NDC: | 49349-997 |
| 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: | 49349-997 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA083677 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120913 |
Package Information of Prednisone
| Package NDC: | 49349-997-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-997-02) |
NDC Information of Prednisone
| NDC Code | 49349-997-02 |
| Proprietary Name | Prednisone |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-997-02) |
| Product NDC | 49349-997 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | PREDNISONE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120913 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | PREDNISONE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
