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Alendronate Sodium
Alendronate Sodium - 51079-942-05 - (Alendronate Sodium)
Drug Information of Alendronate Sodium
| Product NDC: | 51079-942 |
| Proprietary Name: | Alendronate Sodium |
| Non Proprietary Name: | Alendronate Sodium |
| Active Ingredient(s): | 70 mg/1 & nbsp; Alendronate Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alendronate Sodium
| Product NDC: | 51079-942 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076584 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111006 |
Package Information of Alendronate Sodium
| Package NDC: | 51079-942-05 |
| Package Description: | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-942-05) > 1 TABLET in 1 BLISTER PACK (51079-942-01) |
NDC Information of Alendronate Sodium
| NDC Code | 51079-942-05 |
| Proprietary Name | Alendronate Sodium |
| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-942-05) > 1 TABLET in 1 BLISTER PACK (51079-942-01) |
| Product NDC | 51079-942 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alendronate Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111006 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | ALENDRONATE SODIUM |
| Strength Number | 70 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
