Drugplain

BONJESTA 20 mg/1

doxylamine succinate and pyridoxine hydrochloride · TABLET, EXTENDED RELEASE · Duchesnay USA, Inc.

No Recall History
Plain English

BONJESTA is a tablet, extended release containing doxylamine succinate and pyridoxine hydrochloride at 20 mg/1, taken oral. Manufactured by Duchesnay USA, Inc..

Key Facts

Brand Name
BONJESTA
Generic Name
doxylamine succinate and pyridoxine hydrochloride
NDC Code (Product)
55494-120
Manufacturer
Duchesnay USA, Inc.
Strength
20 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
NDA209661
Marketing Start
02/19/2018

Recall History

No Recall History

Frequently Asked Questions

What is BONJESTA used for?

BONJESTA contains doxylamine succinate and pyridoxine hydrochloride. It is a tablet, extended release taken oral. Consult your doctor for specific uses.

Is BONJESTA a controlled substance?

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

What is the generic name for BONJESTA?

The generic name for BONJESTA is doxylamine succinate and pyridoxine hydrochloride. There are 8 other brand versions of doxylamine succinate and pyridoxine hydrochloride.

What is the NDC code for BONJESTA 20 mg/1?

The NDC (National Drug Code) for BONJESTA 20 mg/1 is 55494-120, listed by Duchesnay USA, Inc..