Product NDC: | 21695-731 |
Proprietary Name: | Hydrocortisone Acetate |
Non Proprietary Name: | HYDROCORTISONE ACETATE |
Active Ingredient(s): | 30 mg/1 & nbsp; HYDROCORTISONE ACETATE |
Administration Route(s): | RECTAL |
Dosage Form(s): | SUPPOSITORY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-731 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20040601 |
Package NDC: | 21695-731-12 |
Package Description: | 12 SUPPOSITORY in 1 BOX (21695-731-12) |
NDC Code | 21695-731-12 |
Proprietary Name | Hydrocortisone Acetate |
Package Description | 12 SUPPOSITORY in 1 BOX (21695-731-12) |
Product NDC | 21695-731 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDROCORTISONE ACETATE |
Dosage Form Name | SUPPOSITORY |
Route Name | RECTAL |
Start Marketing Date | 20040601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Rebel Distributors Corp |
Substance Name | HYDROCORTISONE ACETATE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |