Guaifenesin Extended Release 1200 mg/1
Guaifenesin · TABLET, EXTENDED RELEASE · PUBLIX SUPER MARKETS, INC
Guaifenesin Extended Release is a tablet, extended release containing guaifenesin at 1200 mg/1, taken oral. Manufactured by PUBLIX SUPER MARKETS, INC.
Key Facts
- Brand Name
- Guaifenesin Extended Release
- Generic Name
- Guaifenesin
- NDC Code (Product)
41415-997- Manufacturer
- PUBLIX SUPER MARKETS, INC
- Strength
- 1200 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA209254
- Drug Class
- Expectorant [EPC]
- Marketing Start
- 12/10/2017
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
Dosage & Administration
Directions do not crush, chew, or break extended-release tablet take with a full glass of water this product can be administered without regard for the timing of meals adults and children 12 years of age and over: 1 extended-release tablet every 12 hours. Do not exceed 2 extended-release tablets in 24 hours. children under 12 years of age: do not use
Warnings
Warnings Do not use for children under 12 years of age Ask a doctor before use if you have persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus) Stop use and ask a doctor if cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Frequently Asked Questions
What is Guaifenesin Extended Release used for?
Guaifenesin Extended Release contains Guaifenesin. It is a tablet, extended release taken oral. Consult your doctor for specific uses.
Is Guaifenesin Extended Release a controlled substance?
Guaifenesin Extended Release is not classified as a controlled substance by the DEA.
What is the generic name for Guaifenesin Extended Release?
The generic name for Guaifenesin Extended Release is Guaifenesin. There are 12 other brand versions of Guaifenesin.
What is the NDC code for Guaifenesin Extended Release 1200 mg/1?
The NDC (National Drug Code) for Guaifenesin Extended Release 1200 mg/1 is 41415-997, listed by PUBLIX SUPER MARKETS, INC.
Other Guaifenesin Brands
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- basic care mucus er600 mg/172288-298
- basic care mucus er max1200 mg/172288-613
- Pharbinex-DM20 mg/173057-381
- Mucus Relief DM Extended Release Caplets30 mg/10536-1161
- MUCUS RELIEF - DM MAXIMUM STRENGTH60 mg/173581-405
- BACZOL EXPECTORANT200 mg/5mL76864-209
- Guaifenesin and Pseudoephedrine HCl600 mg/179481-1002
- Meijer Adult Mucus Plus chest congestion200 mg/10mL79481-7430
- Tussin Mucus and Chest Congestion Sugar Free200 mg/10mL82568-0012
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)