NDC 68788-8825 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 75 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-8825
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216044
- Marketed since
- February 10, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8825-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-3) | Feb 10, 2025 |
| 68788-8825-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-6) | Feb 10, 2025 |
| 68788-8825-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-9) | Feb 10, 2025 |
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