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SELENIUM SULFIDE
SELENIUM SULFIDE - 54868-1362-1 - (SELENIUM SULFIDE)
Drug Information of SELENIUM SULFIDE
| Product NDC: | 54868-1362 |
| Proprietary Name: | SELENIUM SULFIDE |
| Non Proprietary Name: | SELENIUM SULFIDE |
| Active Ingredient(s): | 2.5 g/100mL & nbsp; SELENIUM SULFIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SELENIUM SULFIDE
| Product NDC: | 54868-1362 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089996 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060925 |
Package Information of SELENIUM SULFIDE
| Package NDC: | 54868-1362-1 |
| Package Description: | 118 mL in 1 BOTTLE (54868-1362-1) |
NDC Information of SELENIUM SULFIDE
| NDC Code | 54868-1362-1 |
| Proprietary Name | SELENIUM SULFIDE |
| Package Description | 118 mL in 1 BOTTLE (54868-1362-1) |
| Product NDC | 54868-1362 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SELENIUM SULFIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060925 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 2.5 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
