Product NDC: | 50458-535 |
Proprietary Name: | Terazol 7 |
Non Proprietary Name: | TERCONAZOLE |
Active Ingredient(s): | 4 mg/g & nbsp; TERCONAZOLE |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50458-535 |
Labeler Name: | Janssen Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019579 |
Marketing Category: | NDA |
Start Marketing Date: | 19871231 |
Package NDC: | 50458-535-01 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (50458-535-01) > 45 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 50458-535-01 |
Proprietary Name | Terazol 7 |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (50458-535-01) > 45 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 50458-535 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TERCONAZOLE |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 19871231 |
Marketing Category Name | NDA |
Labeler Name | Janssen Pharmaceuticals, Inc. |
Substance Name | TERCONAZOLE |
Strength Number | 4 |
Strength Unit | mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |