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Fosamax
Fosamax - 54868-3857-0 - (alendronate sodium)
Drug Information of Fosamax
| Product NDC: | 54868-3857 |
| Proprietary Name: | Fosamax |
| Non Proprietary Name: | alendronate sodium |
| Active Ingredient(s): | 10 mg/1 & nbsp; alendronate sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fosamax
| Product NDC: | 54868-3857 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020560 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961219 |
Package Information of Fosamax
| Package NDC: | 54868-3857-0 |
| Package Description: | 30 TABLET, COATED in 1 BOTTLE (54868-3857-0) |
NDC Information of Fosamax
| NDC Code | 54868-3857-0 |
| Proprietary Name | Fosamax |
| Package Description | 30 TABLET, COATED in 1 BOTTLE (54868-3857-0) |
| Product NDC | 54868-3857 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alendronate sodium |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 19961219 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | ALENDRONATE SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
