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RAYOS
RAYOS - 75987-022-70 - (prednisone)
Drug Information of RAYOS
| Product NDC: | 75987-022 |
| Proprietary Name: | RAYOS |
| Non Proprietary Name: | prednisone |
| Active Ingredient(s): | 5 mg/1 & nbsp; prednisone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RAYOS
| Product NDC: | 75987-022 |
| Labeler Name: | Horizon Pharma Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202020 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120727 |
Package Information of RAYOS
| Package NDC: | 75987-022-70 |
| Package Description: | 1 BOTTLE in 1 CARTON (75987-022-70) > 7 TABLET, DELAYED RELEASE in 1 BOTTLE |
NDC Information of RAYOS
| NDC Code | 75987-022-70 |
| Proprietary Name | RAYOS |
| Package Description | 1 BOTTLE in 1 CARTON (75987-022-70) > 7 TABLET, DELAYED RELEASE in 1 BOTTLE |
| Product NDC | 75987-022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | prednisone |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120727 |
| Marketing Category Name | NDA |
| Labeler Name | Horizon Pharma Inc. |
| Substance Name | PREDNISONE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
