Product NDC: | 0062-5351 |
Proprietary Name: | Terazol 3 |
Non Proprietary Name: | TERCONAZOLE |
Active Ingredient(s): | 80 mg/1 & nbsp; TERCONAZOLE |
Administration Route(s): | VAGINAL |
Dosage Form(s): | SUPPOSITORY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0062-5351 |
Labeler Name: | Ortho-McNeil-Janssen Pharmaceutical |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019641 |
Marketing Category: | NDA |
Start Marketing Date: | 19880627 |
Package NDC: | 0062-5351-01 |
Package Description: | 3 SUPPOSITORY in 1 DOSE PACK (0062-5351-01) |
NDC Code | 0062-5351-01 |
Proprietary Name | Terazol 3 |
Package Description | 3 SUPPOSITORY in 1 DOSE PACK (0062-5351-01) |
Product NDC | 0062-5351 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TERCONAZOLE |
Dosage Form Name | SUPPOSITORY |
Route Name | VAGINAL |
Start Marketing Date | 19880627 |
Marketing Category Name | NDA |
Labeler Name | Ortho-McNeil-Janssen Pharmaceutical |
Substance Name | TERCONAZOLE |
Strength Number | 80 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |