NDC 46708-434 – Venlafaxine
Venlafaxine Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC46708-434
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078932
- Marketed since
- October 1, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 100 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 46708-434-30 | 30 TABLET in 1 BOTTLE (46708-434-30) | Oct 1, 2015 |
| 46708-434-31 | 100 TABLET in 1 BOTTLE (46708-434-31) | Oct 1, 2015 |
| 46708-434-91 | 1000 TABLET in 1 BOTTLE (46708-434-91) | Oct 1, 2015 |
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- 50090-4865 Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · A-S Medication Solutions
- 62332-010 Venlafaxine Hydrochloride 50 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 62332-011 Venlafaxine Hydrochloride 75 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 62332-012 Venlafaxine Hydrochloride 100 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 62332-009 Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 62332-008 Venlafaxine Hydrochloride 25 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 46708-433 Venlafaxine Hydrochloride 75 mg/1 · Tablet · Alembic Pharmaceuticals Limited
- 46708-431 Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · Alembic Pharmaceuticals Limited
- 46708-430 Venlafaxine Hydrochloride 25 mg/1 · Tablet · Alembic Pharmaceuticals Limited