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Mometasone Furoate
Mometasone Furoate - 0115-1469-52 - (Mometasone Furoate)
Drug Information of Mometasone Furoate
| Product NDC: | 0115-1469 |
| Proprietary Name: | Mometasone Furoate |
| Non Proprietary Name: | Mometasone Furoate |
| Active Ingredient(s): | 1 mg/g & nbsp; Mometasone Furoate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mometasone Furoate
| Product NDC: | 0115-1469 |
| Labeler Name: | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076481 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031114 |
Package Information of Mometasone Furoate
| Package NDC: | 0115-1469-52 |
| Package Description: | 1 TUBE in 1 CARTON (0115-1469-52) > 15 g in 1 TUBE |
NDC Information of Mometasone Furoate
| NDC Code | 0115-1469-52 |
| Proprietary Name | Mometasone Furoate |
| Package Description | 1 TUBE in 1 CARTON (0115-1469-52) > 15 g in 1 TUBE |
| Product NDC | 0115-1469 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mometasone Furoate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20031114 |
| Marketing Category Name | ANDA |
| Labeler Name | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
| Substance Name | MOMETASONE FUROATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA] |
