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Vandazole
Vandazole - 0245-0860-70 - (Metronidazole)
Drug Information of Vandazole
| Product NDC: | 0245-0860 |
| Proprietary Name: | Vandazole |
| Non Proprietary Name: | Metronidazole |
| Active Ingredient(s): | 7.5 mg/g & nbsp; Metronidazole |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vandazole
| Product NDC: | 0245-0860 |
| Labeler Name: | Upsher-Smith Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021806 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20051004 |
Package Information of Vandazole
| Package NDC: | 0245-0860-70 |
| Package Description: | 70 g in 1 TUBE, WITH APPLICATOR (0245-0860-70) |
NDC Information of Vandazole
| NDC Code | 0245-0860-70 |
| Proprietary Name | Vandazole |
| Package Description | 70 g in 1 TUBE, WITH APPLICATOR (0245-0860-70) |
| Product NDC | 0245-0860 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Metronidazole |
| Dosage Form Name | GEL |
| Route Name | VAGINAL |
| Start Marketing Date | 20051004 |
| Marketing Category Name | NDA |
| Labeler Name | Upsher-Smith Laboratories, Inc. |
| Substance Name | METRONIDAZOLE |
| Strength Number | 7.5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Nitroimidazole Antimicrobial [EPC],Nitroimidazoles [Chemical/Ingredient] |
