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sunmark
sunmark - 49348-379-54 - (Clotrimazole)
Drug Information of sunmark
| Product NDC: | 49348-379 |
| Proprietary Name: | sunmark |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | 2 g/100g & nbsp; Clotrimazole |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark
| Product NDC: | 49348-379 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021143 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20000412 |
Package Information of sunmark
| Package NDC: | 49348-379-54 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (49348-379-54) > 21 g in 1 TUBE, WITH APPLICATOR |
NDC Information of sunmark
| NDC Code | 49348-379-54 |
| Proprietary Name | sunmark |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (49348-379-54) > 21 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 49348-379 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | CREAM |
| Route Name | VAGINAL |
| Start Marketing Date | 20000412 |
| Marketing Category Name | NDA |
| Labeler Name | McKesson |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
