Product NDC: | 49348-522 |
Proprietary Name: | sunmark |
Non Proprietary Name: | Hydrocortisone |
Active Ingredient(s): | 1 g/100g & nbsp; Hydrocortisone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49348-522 |
Labeler Name: | McKesson |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19891003 |
Package NDC: | 49348-522-72 |
Package Description: | 1 TUBE in 1 CARTON (49348-522-72) > 28.4 g in 1 TUBE |
NDC Code | 49348-522-72 |
Proprietary Name | sunmark |
Package Description | 1 TUBE in 1 CARTON (49348-522-72) > 28.4 g in 1 TUBE |
Product NDC | 49348-522 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Hydrocortisone |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 19891003 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | McKesson |
Substance Name | HYDROCORTISONE |
Strength Number | 1 |
Strength Unit | g/100g |
Pharmaceutical Classes |