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Entex S
Entex S - 66992-290-04 - (Dextromethorphan Hydrobromide)
Drug Information of Entex S
| Product NDC: | 66992-290 |
| Proprietary Name: | Entex S |
| Non Proprietary Name: | Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 20 mg/5mL & nbsp; Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Entex S
| Product NDC: | 66992-290 |
| Labeler Name: | WraSer Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110830 |
Package Information of Entex S
| Package NDC: | 66992-290-04 |
| Package Description: | 118 mL in 1 BOTTLE (66992-290-04) |
NDC Information of Entex S
| NDC Code | 66992-290-04 |
| Proprietary Name | Entex S |
| Package Description | 118 mL in 1 BOTTLE (66992-290-04) |
| Product NDC | 66992-290 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110830 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WraSer Pharmaceuticals, LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 20 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
