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Medisilke
Medisilke - 65588-2230-3 - (HYDROQUINONE)
Drug Information of Medisilke
| Product NDC: | 65588-2230 |
| Proprietary Name: | Medisilke |
| Non Proprietary Name: | HYDROQUINONE |
| Active Ingredient(s): | 2 g/100g & nbsp; HYDROQUINONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Medisilke
| Product NDC: | 65588-2230 |
| Labeler Name: | New GPC, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091201 |
Package Information of Medisilke
| Package NDC: | 65588-2230-3 |
| Package Description: | 1 TUBE in 1 CARTON (65588-2230-3) > 20 g in 1 TUBE |
NDC Information of Medisilke
| NDC Code | 65588-2230-3 |
| Proprietary Name | Medisilke |
| Package Description | 1 TUBE in 1 CARTON (65588-2230-3) > 20 g in 1 TUBE |
| Product NDC | 65588-2230 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROQUINONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20091201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | New GPC, Inc. |
| Substance Name | HYDROQUINONE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
