NDC 42799-963 – Venlafaxine hydrochloride, extended release
Venlafaxine Hydrochloride 225 mg/1 · Tablet · Oral
Product NDC42799-963
Product details
- Brand name
- Venlafaxine hydrochloride, extended release
- Generic name
- Venlafaxine hydrochloride, extended release
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209193
- Marketed since
- March 15, 2023
- Marketing end
- September 30, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 225 mg/1
Uses, dosage, side effects and warnings for Venlafaxine hydrochloride, extended release →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 42799-963-01 | 30 TABLET in 1 BOTTLE (42799-963-01) | Mar 15, 2023 |
| 42799-963-02 | 90 TABLET in 1 BOTTLE (42799-963-02) | Mar 15, 2023 |
Other Venlafaxine hydrochloride, extended release products
- 42799-962 Venlafaxine Hydrochloride 150 mg/1 · Tablet · Edenbridge Pharmaceuticals LLC.