NDC 46708-792 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 37.5 mg/1 · Capsule, Extended Release · Oral
Product NDC46708-792
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA217767
- Marketed since
- June 10, 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 46708-792-30 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-30) | Jun 10, 2024 |
| 46708-792-31 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-31) | Jun 10, 2024 |
| 46708-792-71 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-71) | Jun 10, 2024 |
| 46708-792-90 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-90) | Jun 10, 2024 |
| 46708-792-91 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (46708-792-91) | Jun 10, 2024 |
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