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Sunmark
Sunmark - 49348-279-72 - (Clotrimazole)
Drug Information of Sunmark
| Product NDC: | 49348-279 |
| Proprietary Name: | Sunmark |
| Non Proprietary Name: | Clotrimazole |
| Active Ingredient(s): | 10 mg/g & nbsp; Clotrimazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark
| Product NDC: | 49348-279 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19930831 |
Package Information of Sunmark
| Package NDC: | 49348-279-72 |
| Package Description: | 1 TUBE in 1 CARTON (49348-279-72) > 30 g in 1 TUBE |
NDC Information of Sunmark
| NDC Code | 49348-279-72 |
| Proprietary Name | Sunmark |
| Package Description | 1 TUBE in 1 CARTON (49348-279-72) > 30 g in 1 TUBE |
| Product NDC | 49348-279 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Clotrimazole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19930831 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | CLOTRIMAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
