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GANITE
GANITE - 66657-301-05 - (Gallium nitrate)
Drug Information of GANITE
| Product NDC: | 66657-301 |
| Proprietary Name: | GANITE |
| Non Proprietary Name: | Gallium nitrate |
| Active Ingredient(s): | 25 mg/mL & nbsp; Gallium nitrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GANITE
| Product NDC: | 66657-301 |
| Labeler Name: | Genta Incorporated |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019961 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030917 |
Package Information of GANITE
| Package NDC: | 66657-301-05 |
| Package Description: | 5 VIAL, SINGLE-USE in 1 CARTON (66657-301-05) > 20 mL in 1 VIAL, SINGLE-USE (66657-301-01) (66657-301-01) |
NDC Information of GANITE
| NDC Code | 66657-301-05 |
| Proprietary Name | GANITE |
| Package Description | 5 VIAL, SINGLE-USE in 1 CARTON (66657-301-05) > 20 mL in 1 VIAL, SINGLE-USE (66657-301-01) (66657-301-01) |
| Product NDC | 66657-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Gallium nitrate |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20030917 |
| Marketing Category Name | NDA |
| Labeler Name | Genta Incorporated |
| Substance Name | GALLIUM NITRATE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
