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FOSAMAX PLUS D
FOSAMAX PLUS D - 0006-0270-21 - (ALENDRONATE SODIUM and CHOLECALCIFEROL)
Drug Information of FOSAMAX PLUS D
| Product NDC: | 0006-0270 |
| Proprietary Name: | FOSAMAX PLUS D |
| Non Proprietary Name: | ALENDRONATE SODIUM and CHOLECALCIFEROL |
| Active Ingredient(s): | 70; 5600 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: | 0006-0270 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021762 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050407 |
Package Information of FOSAMAX PLUS D
| Package NDC: | 0006-0270-21 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0006-0270-21) > 10 TABLET in 1 BLISTER PACK (0006-0270-01) |
NDC Information of FOSAMAX PLUS D
| NDC Code | 0006-0270-21 |
| Proprietary Name | FOSAMAX PLUS D |
| Package Description | 2 BLISTER PACK in 1 CARTON (0006-0270-21) > 10 TABLET in 1 BLISTER PACK (0006-0270-01) |
| Product NDC | 0006-0270 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ALENDRONATE SODIUM and CHOLECALCIFEROL |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050407 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | ALENDRONATE SODIUM; CHOLECALCIFEROL |
| Strength Number | 70; 5600 |
| Strength Unit | mg/1; [iU]/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient],Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |
