Home
>
National Drug Code (NDC)
>
Cheratussin AC
Cheratussin AC - 21695-421-04 - (codeine phosphate and guaifenesin)
Drug Information of Cheratussin AC
| Product NDC: | 21695-421 |
| Proprietary Name: | Cheratussin AC |
| Non Proprietary Name: | codeine phosphate and guaifenesin |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; codeine phosphate and guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cheratussin AC
| Product NDC: | 21695-421 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19960901 |
Package Information of Cheratussin AC
| Package NDC: | 21695-421-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (21695-421-04) |
NDC Information of Cheratussin AC
| NDC Code | 21695-421-04 |
| Proprietary Name | Cheratussin AC |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (21695-421-04) |
| Product NDC | 21695-421 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | codeine phosphate and guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19960901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | CODEINE PHOSPHATE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
