NDC 68001-496 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 37.5 mg/1 · Tablet, Extended Release · Oral
Product NDC68001-496
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214419
- Marketed since
- April 30, 2021
- Listing expires
- December 31, 2026
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-496-04 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-496-04) | Apr 30, 2021 |
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