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Pramoxine hydrochloride
Pramoxine hydrochloride - 51862-180-15 - (Pramoxine hydrochloride)
Drug Information of Pramoxine hydrochloride
| Product NDC: | 51862-180 |
| Proprietary Name: | Pramoxine hydrochloride |
| Non Proprietary Name: | Pramoxine hydrochloride |
| Active Ingredient(s): | 10 mg/g & nbsp; Pramoxine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pramoxine hydrochloride
| Product NDC: | 51862-180 |
| Labeler Name: | Libertas Pharma, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111031 |
Package Information of Pramoxine hydrochloride
| Package NDC: | 51862-180-15 |
| Package Description: | 1 CONTAINER in 1 CARTON (51862-180-15) > 15 g in 1 CONTAINER |
NDC Information of Pramoxine hydrochloride
| NDC Code | 51862-180-15 |
| Proprietary Name | Pramoxine hydrochloride |
| Package Description | 1 CONTAINER in 1 CARTON (51862-180-15) > 15 g in 1 CONTAINER |
| Product NDC | 51862-180 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Pramoxine hydrochloride |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111031 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Libertas Pharma, Inc. |
| Substance Name | PRAMOXINE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
