Home
>
National Drug Code (NDC)
>
Rx Act Tussin CF
Rx Act Tussin CF - 37808-516-34 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of Rx Act Tussin CF
| Product NDC: | 37808-516 |
| Proprietary Name: | Rx Act Tussin CF |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 10; 100; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rx Act Tussin CF
| Product NDC: | 37808-516 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19960718 |
Package Information of Rx Act Tussin CF
| Package NDC: | 37808-516-34 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-516-34) > 237 mL in 1 BOTTLE |
NDC Information of Rx Act Tussin CF
| NDC Code | 37808-516-34 |
| Proprietary Name | Rx Act Tussin CF |
| Package Description | 1 BOTTLE in 1 CARTON (37808-516-34) > 237 mL in 1 BOTTLE |
| Product NDC | 37808-516 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19960718 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | H E B |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
