Product NDC: | 68462-385 |
Proprietary Name: | Mometasone Furoate |
Non Proprietary Name: | Mometasone Furoate |
Active Ingredient(s): | 1 mg/mL & nbsp; Mometasone Furoate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68462-385 |
Labeler Name: | Glenmark Generics Inc., USA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090506 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100809 |
Package NDC: | 68462-385-37 |
Package Description: | 30 mL in 1 TUBE (68462-385-37) |
NDC Code | 68462-385-37 |
Proprietary Name | Mometasone Furoate |
Package Description | 30 mL in 1 TUBE (68462-385-37) |
Product NDC | 68462-385 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Mometasone Furoate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100809 |
Marketing Category Name | ANDA |
Labeler Name | Glenmark Generics Inc., USA |
Substance Name | MOMETASONE FUROATE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA] |