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Dulera
Dulera - 0085-7206-01 - (mometasone furoate and formoterol fumarate dihydrate)
Drug Information of Dulera
| Product NDC: | 0085-7206 |
| Proprietary Name: | Dulera |
| Non Proprietary Name: | mometasone furoate and formoterol fumarate dihydrate |
| Active Ingredient(s): | 5; 100 ug/1; ug/1 & nbsp; mometasone furoate and formoterol fumarate dihydrate |
| Administration Route(s): | RESPIRATORY (INHALATION) |
| Dosage Form(s): | AEROSOL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dulera
| Product NDC: | 0085-7206 |
| Labeler Name: | Merck Sharp & Dohme Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022518 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100622 |
Package Information of Dulera
| Package NDC: | 0085-7206-01 |
| Package Description: | 1 CANISTER in 1 CARTON (0085-7206-01) > 120 AEROSOL in 1 CANISTER |
NDC Information of Dulera
| NDC Code | 0085-7206-01 |
| Proprietary Name | Dulera |
| Package Description | 1 CANISTER in 1 CARTON (0085-7206-01) > 120 AEROSOL in 1 CANISTER |
| Product NDC | 0085-7206 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mometasone furoate and formoterol fumarate dihydrate |
| Dosage Form Name | AEROSOL |
| Route Name | RESPIRATORY (INHALATION) |
| Start Marketing Date | 20100622 |
| Marketing Category Name | NDA |
| Labeler Name | Merck Sharp & Dohme Corp. |
| Substance Name | FORMOTEROL FUMARATE DIHYDRATE; MOMETASONE FUROATE |
| Strength Number | 5; 100 |
| Strength Unit | ug/1; ug/1 |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid Hormone Receptor Agonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |
