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ALENDRONATE SODIUM
ALENDRONATE SODIUM - 24658-162-73 - (ALENDRONATE SODIUM)
Drug Information of ALENDRONATE SODIUM
| Product NDC: | 24658-162 |
| Proprietary Name: | ALENDRONATE SODIUM |
| Non Proprietary Name: | ALENDRONATE SODIUM |
| Active Ingredient(s): | 35 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: | 24658-162 |
| Labeler Name: | Blu Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090258 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130205 |
Package Information of ALENDRONATE SODIUM
| Package NDC: | 24658-162-73 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (24658-162-73) > 4 TABLET in 1 BLISTER PACK (24658-162-71) |
NDC Information of ALENDRONATE SODIUM
| NDC Code | 24658-162-73 |
| Proprietary Name | ALENDRONATE SODIUM |
| Package Description | 3 BLISTER PACK in 1 CARTON (24658-162-73) > 4 TABLET in 1 BLISTER PACK (24658-162-71) |
| Product NDC | 24658-162 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ALENDRONATE SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130205 |
| Marketing Category Name | ANDA |
| Labeler Name | Blu Pharmaceuticals, LLC |
| Substance Name | ALENDRONATE SODIUM |
| Strength Number | 35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
