NDC 47335-794 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Oral
Product NDC47335-794
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA091272
- Marketed since
- February 15, 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 47335-794-08 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08) | Feb 15, 2019 |
| 47335-794-13 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13) | Feb 15, 2019 |
| 47335-794-81 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81) | Aug 15, 2019 |
| 47335-794-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83) | Feb 15, 2019 |
| 47335-794-88 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88) | Feb 15, 2019 |
| 47335-794-99 | 5 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Feb 15, 2019 |
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