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Duract
Duract - 62750-042-10 - (Dextromethorphan Hydrobromide)
Drug Information of Duract
| Product NDC: | 62750-042 |
| Proprietary Name: | Duract |
| Non Proprietary Name: | Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 30 mg/1 & nbsp; Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Duract
| Product NDC: | 62750-042 |
| Labeler Name: | Matrixx Initiatives, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110801 |
Package Information of Duract
| Package NDC: | 62750-042-10 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (62750-042-10) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of Duract
| NDC Code | 62750-042-10 |
| Proprietary Name | Duract |
| Package Description | 2 BLISTER PACK in 1 CARTON (62750-042-10) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 62750-042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Matrixx Initiatives, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
