NDC 47335-758 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC47335-758
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
- December 15, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 47335-758-08 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-08) | Dec 15, 2014 |
| 47335-758-18 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-18) | Dec 15, 2014 |
| 47335-758-81 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-81) | Dec 15, 2014 |
| 47335-758-83 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-83) | Dec 15, 2014 |
| 47335-758-88 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-88) | Dec 15, 2014 |
| 47335-758-99 | 2 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-758-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | Mar 29, 2019 |
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