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DM MAX
DM MAX - 68016-222-00 - (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN)
Drug Information of DM MAX
| Product NDC: | 68016-222 |
| Proprietary Name: | DM MAX |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Active Ingredient(s): | 20; 400 mg/20mL; mg/20mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DM MAX
| Product NDC: | 68016-222 |
| Labeler Name: | Chain Drug Consortium, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130101 |
Package Information of DM MAX
| Package NDC: | 68016-222-00 |
| Package Description: | 177 mL in 1 BOTTLE (68016-222-00) |
NDC Information of DM MAX
| NDC Code | 68016-222-00 |
| Proprietary Name | DM MAX |
| Package Description | 177 mL in 1 BOTTLE (68016-222-00) |
| Product NDC | 68016-222 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Chain Drug Consortium, LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/20mL; mg/20mL |
| Pharmaceutical Classes |
