Drugplain

Altituss 15 mg/7.5mL

Dextromethorphan HBr, Guaifenesin · LIQUID · Alternative Pharmacal Corporation

No Recall History
Plain English

Altituss is a liquid containing dextromethorphan hbr, guaifenesin at 15 mg/7.5mL, taken oral. Manufactured by Alternative Pharmacal Corporation.

Key Facts

Brand Name
Altituss
Generic Name
Dextromethorphan HBr, Guaifenesin
NDC Code (Product)
53163-113
Manufacturer
Alternative Pharmacal Corporation
Strength
15 mg/7.5mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Application #
M012
Drug Class
Expectorant [EPC]
Marketing Start
03/01/2015

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

dehydration1 reports
drug ineffective1 reports
dry skin1 reports
feeling hot1 reports
hyperhidrosis1 reports
limb discomfort1 reports
speech disorder1 reports
tremor1 reports

Frequently Asked Questions

What is Altituss used for?

Altituss contains Dextromethorphan HBr, Guaifenesin. It is a liquid taken oral. Consult your doctor for specific uses.

Is Altituss a controlled substance?

Altituss is not classified as a controlled substance by the DEA.

What is the generic name for Altituss?

The generic name for Altituss is Dextromethorphan HBr, Guaifenesin. There are 12 other brand versions of Dextromethorphan HBr, Guaifenesin.

What is the NDC code for Altituss 15 mg/7.5mL?

The NDC (National Drug Code) for Altituss 15 mg/7.5mL is 53163-113, listed by Alternative Pharmacal Corporation.