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Mometasone Furoate
Mometasone Furoate - 0781-7068-19 - (Mometasone Furoate)
Drug Information of Mometasone Furoate
| Product NDC: | 0781-7068 |
| 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: | 0781-7068 |
| Labeler Name: | Sandoz |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076481 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20031114 |
Package Information of Mometasone Furoate
| Package NDC: | 0781-7068-19 |
| Package Description: | 45 g in 1 TUBE (0781-7068-19) |
NDC Information of Mometasone Furoate
| NDC Code | 0781-7068-19 |
| Proprietary Name | Mometasone Furoate |
| Package Description | 45 g in 1 TUBE (0781-7068-19) |
| Product NDC | 0781-7068 |
| 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 | Sandoz |
| Substance Name | MOMETASONE FUROATE |
| Strength Number | 1 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
