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Halonate
Halonate - 68712-034-01 - (Halobetasol)
Drug Information of Halonate
| Product NDC: | 68712-034 |
| Proprietary Name: | Halonate |
| Non Proprietary Name: | Halobetasol |
| Active Ingredient(s): | .5 mg/g & nbsp; Halobetasol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Halonate
| Product NDC: | 68712-034 |
| Labeler Name: | Innocutis Holding LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077721 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090801 |
Package Information of Halonate
| Package NDC: | 68712-034-01 |
| Package Description: | 50 g in 1 TUBE (68712-034-01) |
NDC Information of Halonate
| NDC Code | 68712-034-01 |
| Proprietary Name | Halonate |
| Package Description | 50 g in 1 TUBE (68712-034-01) |
| Product NDC | 68712-034 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Halobetasol |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20090801 |
| Marketing Category Name | ANDA |
| Labeler Name | Innocutis Holding LLC |
| Substance Name | HALOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
