NDC 31722-004 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 150 mg/1 · Capsule, Extended Release · Oral
Product NDC31722-004
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212277
- Marketed since
- July 8, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 31722-004-01 | 10 BLISTER PACK in 1 CARTON (31722-004-01) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK | Jul 8, 2019 |
| 31722-004-05 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-05) | Jul 8, 2019 |
| 31722-004-30 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-30) | Jul 8, 2019 |
| 31722-004-90 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-004-90) | Jul 8, 2019 |
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