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Alendronate Sodium
Alendronate Sodium - 16252-599-02 - (alendronate sodium)
Drug Information of Alendronate Sodium
| Product NDC: | 16252-599 |
| 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: | 16252-599 |
| Labeler Name: | Cobalt Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076984 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091023 |
Package Information of Alendronate Sodium
| Package NDC: | 16252-599-02 |
| Package Description: | 3 BLISTER PACK in 1 BOX, UNIT-DOSE (16252-599-02) > 4 TABLET in 1 BLISTER PACK |
NDC Information of Alendronate Sodium
| NDC Code | 16252-599-02 |
| Proprietary Name | Alendronate Sodium |
| Package Description | 3 BLISTER PACK in 1 BOX, UNIT-DOSE (16252-599-02) > 4 TABLET in 1 BLISTER PACK |
| Product NDC | 16252-599 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alendronate sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091023 |
| Marketing Category Name | ANDA |
| Labeler Name | Cobalt Laboratories Inc. |
| Substance Name | ALENDRONATE SODIUM |
| Strength Number | 35 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
