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SUNMARK TIOCONAZOLE 1
SUNMARK TIOCONAZOLE 1 - 49348-508-59 - (Tioconazole)
Drug Information of SUNMARK TIOCONAZOLE 1
| Product NDC: | 49348-508 |
| Proprietary Name: | SUNMARK TIOCONAZOLE 1 |
| Non Proprietary Name: | Tioconazole |
| Active Ingredient(s): | 6.5 g/100g & nbsp; Tioconazole |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNMARK TIOCONAZOLE 1
| Product NDC: | 49348-508 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075915 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071218 |
Package Information of SUNMARK TIOCONAZOLE 1
| Package NDC: | 49348-508-59 |
| Package Description: | 1 APPLICATOR in 1 CARTON (49348-508-59) > 4.6 g in 1 APPLICATOR |
NDC Information of SUNMARK TIOCONAZOLE 1
| NDC Code | 49348-508-59 |
| Proprietary Name | SUNMARK TIOCONAZOLE 1 |
| Package Description | 1 APPLICATOR in 1 CARTON (49348-508-59) > 4.6 g in 1 APPLICATOR |
| Product NDC | 49348-508 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tioconazole |
| Dosage Form Name | OINTMENT |
| Route Name | VAGINAL |
| Start Marketing Date | 20071218 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | TIOCONAZOLE |
| Strength Number | 6.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
