NDC 43598-999 – Venlafaxine hydrochloride
Venlafaxine Hydrochloride 37.5 mg/1 · Capsule, Extended Release · Oral
Product NDC43598-999
Product details
- Brand name
- Venlafaxine hydrochloride
- Generic name
- Venlafaxine hydrochloride
- Labeler
- Dr.Reddys Laboratories Inc
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078421
- Marketed since
- September 9, 2024
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 43598-999-10 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-999-10) | Sep 9, 2024 |
| 43598-999-30 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-999-30) | Sep 9, 2024 |
| 43598-999-90 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-999-90) | Sep 9, 2024 |
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