Sambrosa Night 9.78 mg/3mL
DOXYLAMINE SUCCINATE · SYRUP · Sambrosa Care, Inc.
Sambrosa Night is a syrup containing doxylamine succinate at 9.78 mg/3mL, taken oral. Manufactured by Sambrosa Care, Inc..
Key Facts
- Brand Name
- Sambrosa Night
- Generic Name
- DOXYLAMINE SUCCINATE
- NDC Code (Product)
60665-003- Manufacturer
- Sambrosa Care, Inc.
- Strength
- 9.78 mg/3mL
- Dosage Form
- SYRUP
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Marketing Start
- 01/10/2020
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 temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: sneezing runny nose itchy, watery eyes itching of the nose or throat
Dosage & Administration
Directions take only as directed always use the provided measurement spoon. A full spoon equals 3mL. adults and children 12 years of age and over: oral dosage is 3 mL every 4 to 6 hours, not to exceed 18 mL in 24 hours, or as directed by a doctor. children under 12 years of age: consult a doctor.
Warnings
Warnings
Frequently Asked Questions
What is Sambrosa Night used for?
Sambrosa Night contains DOXYLAMINE SUCCINATE. It is a syrup taken oral. Consult your doctor for specific uses.
Is Sambrosa Night a controlled substance?
Sambrosa Night is not classified as a controlled substance by the DEA.
What is the generic name for Sambrosa Night?
The generic name for Sambrosa Night is DOXYLAMINE SUCCINATE. There are 12 other brand versions of DOXYLAMINE SUCCINATE.
What is the NDC code for Sambrosa Night 9.78 mg/3mL?
The NDC (National Drug Code) for Sambrosa Night 9.78 mg/3mL is 60665-003, listed by Sambrosa Care, 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)