| 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: | 0003-0249-20 |
| Package Description: | 60 mL in 1 BOTTLE, PLASTIC (0003-0249-20) |
| NDC Code | 0003-0249-20 |
| Proprietary Name | HALOG |
| Package Description | 60 mL in 1 BOTTLE, PLASTIC (0003-0249-20) |
| 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] |