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: | 64543-178-24 |
Package Description: | 24 TABLET in 1 BOTTLE (64543-178-24) |
NDC Code | 64543-178-24 |
Proprietary Name | Certuss-D |
Package Description | 24 TABLET in 1 BOTTLE (64543-178-24) |
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 |