Product NDC: | 0003-0249 |
Proprietary Name: | HALOG |
Non Proprietary Name: | Halcinonide |
Active Ingredient(s): | 1 mg/mL & nbsp; Halcinonide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0003-0249 |
Labeler Name: | E.R. Squibb & Sons, L.L.C. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017823 |
Marketing Category: | NDA |
Start Marketing Date: | 20090101 |
Package NDC: | 0003-0249-15 |
Package Description: | 20 mL in 1 BOTTLE, PLASTIC (0003-0249-15) |
NDC Code | 0003-0249-15 |
Proprietary Name | HALOG |
Package Description | 20 mL in 1 BOTTLE, PLASTIC (0003-0249-15) |
Product NDC | 0003-0249 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Halcinonide |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20090101 |
Marketing Category Name | NDA |
Labeler Name | E.R. Squibb & Sons, L.L.C. |
Substance Name | HALCINONIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |