Home
>
National Drug Code (NDC)
>
Hydrocortisone Butyrate
Hydrocortisone Butyrate - 21695-971-15 - (Hydrocortisone Butyrate)
Drug Information of Hydrocortisone Butyrate
| Product NDC: | 21695-971 |
| Proprietary Name: | Hydrocortisone Butyrate |
| Non Proprietary Name: | Hydrocortisone Butyrate |
| Active Ingredient(s): | 1 mg/g & nbsp; Hydrocortisone Butyrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone Butyrate
| Product NDC: | 21695-971 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018514 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090901 |
Package Information of Hydrocortisone Butyrate
| Package NDC: | 21695-971-15 |
| Package Description: | 1 TUBE in 1 CARTON (21695-971-15) > 15 g in 1 TUBE |
NDC Information of Hydrocortisone Butyrate
| NDC Code | 21695-971-15 |
| Proprietary Name | Hydrocortisone Butyrate |
| Package Description | 1 TUBE in 1 CARTON (21695-971-15) > 15 g in 1 TUBE |
| Product NDC | 21695-971 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Butyrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | HYDROCORTISONE BUTYRATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
