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IBANDRONATE SODIUM
IBANDRONATE SODIUM - 60505-2795-0 - (IBANDRONATE SODIUM)
Drug Information of IBANDRONATE SODIUM
| Product NDC: | 60505-2795 |
| Proprietary Name: | IBANDRONATE SODIUM |
| Non Proprietary Name: | IBANDRONATE SODIUM |
| Active Ingredient(s): | 150 mg/1 & nbsp; IBANDRONATE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBANDRONATE SODIUM
| Product NDC: | 60505-2795 |
| Labeler Name: | Apotex Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078948 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120319 |
Package Information of IBANDRONATE SODIUM
| Package NDC: | 60505-2795-0 |
| Package Description: | 3 BLISTER PACK in 1 PACKAGE (60505-2795-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of IBANDRONATE SODIUM
| NDC Code | 60505-2795-0 |
| Proprietary Name | IBANDRONATE SODIUM |
| Package Description | 3 BLISTER PACK in 1 PACKAGE (60505-2795-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 60505-2795 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | IBANDRONATE SODIUM |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120319 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp |
| Substance Name | IBANDRONATE SODIUM |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
