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Scytera
Scytera - 63094-0801-1 - (coal tar foam, 2%)
Drug Information of Scytera
| Product NDC: | 63094-0801 |
| Proprietary Name: | Scytera |
| Non Proprietary Name: | coal tar foam, 2% |
| Active Ingredient(s): | 20 mg/g & nbsp; coal tar foam, 2% |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Scytera
| Product NDC: | 63094-0801 |
| Labeler Name: | DPT Laboratories, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20081031 |
Package Information of Scytera
| Package NDC: | 63094-0801-1 |
| Package Description: | 1 CAN in 1 CARTON (63094-0801-1) > 100 g in 1 CAN |
NDC Information of Scytera
| NDC Code | 63094-0801-1 |
| Proprietary Name | Scytera |
| Package Description | 1 CAN in 1 CARTON (63094-0801-1) > 100 g in 1 CAN |
| Product NDC | 63094-0801 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | coal tar foam, 2% |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20081031 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DPT Laboratories, Ltd. |
| Substance Name | COAL TAR |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
