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Boniva
Boniva - 0004-0186-98 - (ibandronate sodium)
Drug Information of Boniva
| Product NDC: | 0004-0186 |
| Proprietary Name: | Boniva |
| 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 Boniva
| Product NDC: | 0004-0186 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021455 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020715 |
Package Information of Boniva
| Package NDC: | 0004-0186-98 |
| Package Description: | 1 BLISTER PACK in 1 BOX (0004-0186-98) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Boniva
| NDC Code | 0004-0186-98 |
| Proprietary Name | Boniva |
| Package Description | 1 BLISTER PACK in 1 BOX (0004-0186-98) > 1 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0004-0186 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ibandronate sodium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020715 |
| Marketing Category Name | NDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | IBANDRONATE SODIUM |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient] |
