NDC 42806-601 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 37.5 mg/1 · Capsule, Extended Release · Oral
Product NDC42806-601
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Epic Pharma, LLC
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214654
- Marketed since
- September 7, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 37.5 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 42806-601-09 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-09) | Sep 7, 2022 |
| 42806-601-10 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-10) | Sep 7, 2022 |
| 42806-601-30 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42806-601-30) | Sep 7, 2022 |
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