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FOSAMAX PLUS D
FOSAMAX PLUS D - 54868-5480-0 - (alendronate sodium and cholecalciferol)
Drug Information of FOSAMAX PLUS D
| Product NDC: | 54868-5480 |
| Proprietary Name: | FOSAMAX PLUS D |
| Non Proprietary Name: | alendronate sodium and cholecalciferol |
| Active Ingredient(s): | 70; 2800 mg/1; [iU]/1 & nbsp; alendronate sodium and cholecalciferol |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FOSAMAX PLUS D
| Product NDC: | 54868-5480 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021762 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051130 |
Package Information of FOSAMAX PLUS D
| Package NDC: | 54868-5480-0 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (54868-5480-0) > 4 TABLET in 1 BLISTER PACK |
NDC Information of FOSAMAX PLUS D
| NDC Code | 54868-5480-0 |
| Proprietary Name | FOSAMAX PLUS D |
| Package Description | 1 BLISTER PACK in 1 CARTON (54868-5480-0) > 4 TABLET in 1 BLISTER PACK |
| Product NDC | 54868-5480 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alendronate sodium and cholecalciferol |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051130 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ALENDRONATE SODIUM; CHOLECALCIFEROL |
| Strength Number | 70; 2800 |
| Strength Unit | mg/1; [iU]/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient],Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |
