NDC 70710-1352 – Venlafaxine
Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Oral
Product NDC70710-1352
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA215622
- Marketed since
- September 1, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 225 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1352-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-1) | Sep 1, 2022 |
| 70710-1352-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-3) | Sep 1, 2022 |
| 70710-1352-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1352-9) | Sep 1, 2022 |
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