NDC 75834-219 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Oral
Product NDC75834-219
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Nivagen Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211323
- Marketed since
- September 6, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 225 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 75834-219-00 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-00) | Sep 6, 2019 |
| 75834-219-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-30) | Sep 6, 2019 |
| 75834-219-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (75834-219-90) | Sep 6, 2019 |
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