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Creomulsion
Creomulsion - 12090-0024-0 - (DEXTROMETHORPHAN HYDROBROMIDE)
Drug Information of Creomulsion
| Product NDC: | 12090-0024 |
| Proprietary Name: | Creomulsion |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE |
| Active Ingredient(s): | 20 mg/15mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Creomulsion
| Product NDC: | 12090-0024 |
| Labeler Name: | Summit Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091230 |
Package Information of Creomulsion
| Package NDC: | 12090-0024-0 |
| Package Description: | 1 BOTTLE in 1 CARTON (12090-0024-0) > 118 mL in 1 BOTTLE (12090-0024-1) |
NDC Information of Creomulsion
| NDC Code | 12090-0024-0 |
| Proprietary Name | Creomulsion |
| Package Description | 1 BOTTLE in 1 CARTON (12090-0024-0) > 118 mL in 1 BOTTLE (12090-0024-1) |
| Product NDC | 12090-0024 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20091230 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Summit Industries, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 20 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |
