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Tussin CF
Tussin CF - 41520-126-04 - (DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of Tussin CF
| Product NDC: | 41520-126 |
| Proprietary Name: | 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 Tussin CF
| Product NDC: | 41520-126 |
| Labeler Name: | American Sales Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090826 |
Package Information of Tussin CF
| Package NDC: | 41520-126-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (41520-126-04) |
NDC Information of Tussin CF
| NDC Code | 41520-126-04 |
| Proprietary Name | Tussin CF |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (41520-126-04) |
| Product NDC | 41520-126 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20090826 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | American Sales Company |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
