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Mometasone Furoate
Mometasone Furoate - 68462-225-17 - (Mometasone furoate)
Drug Information of Mometasone Furoate
| Product NDC: | 68462-225 |
| 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: | 68462-225 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078571 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080528 |
Package Information of Mometasone Furoate
| Package NDC: | 68462-225-17 |
| Package Description: | 15 g in 1 TUBE (68462-225-17) |
NDC Information of Mometasone Furoate
| NDC Code | 68462-225-17 |
| Proprietary Name | Mometasone Furoate |
| Package Description | 15 g in 1 TUBE (68462-225-17) |
| Product NDC | 68462-225 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mometasone furoate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20080528 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| 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] |
