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SUNMARK TUSSIN CF
SUNMARK TUSSIN CF - 49348-737-37 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of SUNMARK TUSSIN CF
| Product NDC: | 49348-737 |
| Proprietary Name: | SUNMARK 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 SUNMARK TUSSIN CF
| Product NDC: | 49348-737 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20060502 |
Package Information of SUNMARK TUSSIN CF
| Package NDC: | 49348-737-37 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-737-37) > 236 mL in 1 BOTTLE |
NDC Information of SUNMARK TUSSIN CF
| NDC Code | 49348-737-37 |
| Proprietary Name | SUNMARK TUSSIN CF |
| Package Description | 1 BOTTLE in 1 CARTON (49348-737-37) > 236 mL in 1 BOTTLE |
| Product NDC | 49348-737 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20060502 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | McKesson |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 100; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
