| Product NDC: | 64543-178 |
| Proprietary Name: | Certuss-D |
| Non Proprietary Name: | Chlophedianol HCl, Guaifenesin and Pseudoephedrine HCl |
| Active Ingredient(s): | 25; 400; 60 mg/1; mg/1; mg/1 & nbsp; Chlophedianol HCl, Guaifenesin and Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64543-178 |
| Labeler Name: | Capellon Pharmaceuticals, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101123 |
| Package NDC: | 64543-178-90 |
| Package Description: | 90 TABLET in 1 BOTTLE (64543-178-90) |
| NDC Code | 64543-178-90 |
| Proprietary Name | Certuss-D |
| Package Description | 90 TABLET in 1 BOTTLE (64543-178-90) |
| Product NDC | 64543-178 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlophedianol HCl, Guaifenesin and Pseudoephedrine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101123 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Capellon Pharmaceuticals, LLC |
| Substance Name | CHLOPHEDIANOL HYDROCHLORIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 25; 400; 60 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |