NDC 42708-194 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 75 mg/1 · Capsule, Extended Release · Oral
Product NDC42708-194
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- QPharma, Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA200834
- Marketed since
- June 1, 2011
- Listing expires
- December 31, 2027
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 42708-194-30 sample | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42708-194-30) | Feb 1, 2026 |
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