NDC 70710-1700 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 150 mg/1 · Capsule, Extended Release · Oral
Product NDC70710-1700
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090174
- Marketed since
- May 18, 2023
- Listing expires
- December 31, 2027
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1700-0 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-0) | May 18, 2023 |
| 70710-1700-3 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-3) | May 18, 2023 |
| 70710-1700-4 | 10 BLISTER PACK in 1 CARTON (70710-1700-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1700-2) | May 18, 2023 |
| 70710-1700-5 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-5) | May 18, 2023 |
| 70710-1700-9 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1700-9) | May 18, 2023 |
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