Product NDC: | 51672-2013 |
Proprietary Name: | Hydrocortisone |
Non Proprietary Name: | Hydrocortisone |
Active Ingredient(s): | 1 g/100g & nbsp; Hydrocortisone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-2013 |
Labeler Name: | Taro Phamaceuticals U.S.A., Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19950823 |
Package NDC: | 51672-2013-1 |
Package Description: | 1 TUBE in 1 CARTON (51672-2013-1) > 14.2 g in 1 TUBE |
NDC Code | 51672-2013-1 |
Proprietary Name | Hydrocortisone |
Package Description | 1 TUBE in 1 CARTON (51672-2013-1) > 14.2 g in 1 TUBE |
Product NDC | 51672-2013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hydrocortisone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19950823 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Taro Phamaceuticals U.S.A., Inc. |
Substance Name | HYDROCORTISONE |
Strength Number | 1 |
Strength Unit | g/100g |
Pharmaceutical Classes |