Ambien 5 mg/1
zolpidem tartrate · TABLET, FILM COATED · Sanofi-Aventis U.S. LLC
Ambien is a tablet, film coated containing zolpidem tartrate at 5 mg/1, taken oral. Manufactured by Sanofi-Aventis U.S. LLC.
Key Facts
- Brand Name
- Ambien
- Generic Name
- zolpidem tartrate
- NDC Code (Product)
0024-5401- Manufacturer
- Sanofi-Aventis U.S. LLC
- Strength
- 5 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- DEA Schedule
- Schedule IV (Controlled)
- Application #
- NDA019908
- Marketing Start
- 04/01/1993
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 Ambien used for?
Ambien contains zolpidem tartrate. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Ambien a controlled substance?
Yes, Ambien is classified as CIV under the DEA Controlled Substances Act.
What is the generic name for Ambien?
The generic name for Ambien is zolpidem tartrate. There are 12 other brand versions of zolpidem tartrate.
What is the NDC code for Ambien 5 mg/1?
The NDC (National Drug Code) for Ambien 5 mg/1 is 0024-5401, listed by Sanofi-Aventis U.S. LLC.
Other Zolpidem Brands
See all →- ZOLPIDEM TARTRATE10 mg/172722-104
- ZOLPIDEM TARTRATE12.5 mg/176420-319
- Zolpidem Tartrate10 mg/180425-0059
- Zolpidem Tartrate10 mg/180425-0153
- Zolpidem Tartrate10 mg/180425-0301
- Zolpidem tartrate12.5 mg/10781-5316
- Zolpidem Tartrate10 mg/150090-3878
- ZOLPIDEM TARTRATE5 mg/155154-1398
- Zolpidem Tartrate5 mg/160687-838
- Zolpidem Tartrate10 mg/162135-779
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)