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Iophen DM NR
Iophen DM NR - 0603-1330-58 - (dextromethorphan and guaifenesin)
Drug Information of Iophen DM NR
| Product NDC: | 0603-1330 |
| Proprietary Name: | Iophen DM NR |
| Non Proprietary Name: | dextromethorphan and guaifenesin |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; dextromethorphan and guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Iophen DM NR
| Product NDC: | 0603-1330 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19970501 |
Package Information of Iophen DM NR
| Package NDC: | 0603-1330-58 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0603-1330-58) |
NDC Information of Iophen DM NR
| NDC Code | 0603-1330-58 |
| Proprietary Name | Iophen DM NR |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (0603-1330-58) |
| Product NDC | 0603-1330 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan and guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19970501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | DEXTROMETHORPHAN; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
