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Sarna
Sarna - 0145-0630-05 - (pramoxine hydrochloride)
Drug Information of Sarna
| Product NDC: | 0145-0630 |
| Proprietary Name: | Sarna |
| Non Proprietary Name: | pramoxine hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; pramoxine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sarna
| Product NDC: | 0145-0630 |
| Labeler Name: | Stiefel Laboratories, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110222 |
Package Information of Sarna
| Package NDC: | 0145-0630-05 |
| Package Description: | 222 mL in 1 BOTTLE, PUMP (0145-0630-05) |
NDC Information of Sarna
| NDC Code | 0145-0630-05 |
| Proprietary Name | Sarna |
| Package Description | 222 mL in 1 BOTTLE, PUMP (0145-0630-05) |
| Product NDC | 0145-0630 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | pramoxine hydrochloride |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110222 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Stiefel Laboratories, Inc |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
