TUSSIN CF 10 mg/5mL
DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE · LIQUID · AptaPharma Inc.
TUSSIN CF is a liquid containing dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride at 10 mg/5mL, taken oral. Manufactured by AptaPharma Inc..
Key Facts
- Brand Name
- TUSSIN CF
- Generic Name
- DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE
- NDC Code (Product)
76281-504- Manufacturer
- AptaPharma Inc.
- Strength
- 10 mg/5mL
- Dosage Form
- LIQUID
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Drug Class
- Expectorant [EPC]
- Marketing Start
- 09/30/2020
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is TUSSIN CF used for?
TUSSIN CF contains DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE. It is a liquid taken oral. Consult your doctor for specific uses.
Is TUSSIN CF a controlled substance?
TUSSIN CF is not classified as a controlled substance by the DEA.
What is the generic name for TUSSIN CF?
The generic name for TUSSIN CF is DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE. There are 12 other brand versions of DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE.
What is the NDC code for TUSSIN CF 10 mg/5mL?
The NDC (National Drug Code) for TUSSIN CF 10 mg/5mL is 76281-504, listed by AptaPharma Inc..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)