venlafaxine hydrochloride, extended release 150 mg/1
venlafaxine hydrochloride, extended release · TABLET · Edenbridge Pharmaceuticals LLC.
venlafaxine hydrochloride, extended release is a tablet containing venlafaxine hydrochloride, extended release at 150 mg/1, taken oral. Manufactured by Edenbridge Pharmaceuticals LLC..
Key Facts
- Brand Name
- venlafaxine hydrochloride, extended release
- Generic Name
- venlafaxine hydrochloride, extended release
- NDC Code (Product)
42799-962- Manufacturer
- Edenbridge Pharmaceuticals LLC.
- Strength
- 150 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA209193
- Marketing Start
- 03/15/2023
Recall History
No Recall HistoryFrequently Asked Questions
What is venlafaxine hydrochloride, extended release used for?
venlafaxine hydrochloride, extended release contains venlafaxine hydrochloride, extended release. It is a tablet taken oral. Consult your doctor for specific uses.
Is venlafaxine hydrochloride, extended release a controlled substance?
venlafaxine hydrochloride, extended release is not classified as a controlled substance by the DEA.
What is the generic name for venlafaxine hydrochloride, extended release?
The generic name for venlafaxine hydrochloride, extended release is venlafaxine hydrochloride, extended release. There are no other listed brand versions of venlafaxine hydrochloride, extended release.
What is the NDC code for venlafaxine hydrochloride, extended release 150 mg/1?
The NDC (National Drug Code) for venlafaxine hydrochloride, extended release 150 mg/1 is 42799-962, listed by Edenbridge Pharmaceuticals LLC..
Other venlafaxine hydrochloride, extended release Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)