NDC 68001-159 – Venlafaxine
Venlafaxine Hydrochloride 50 mg/1 · Tablet · Oral
Product NDC68001-159
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077653
- Marketed since
- November 25, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 50 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-159-00 | 100 TABLET in 1 BOTTLE (68001-159-00) | Nov 25, 2013 |
Other Venlafaxine products
- 50090-4865 Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · A-S Medication Solutions
- 50090-4715 Venlafaxine Hydrochloride 75 mg/1 · Tablet · A-S Medication Solutions
- 50090-2408 Venlafaxine Hydrochloride 75 mg/1 · Tablet · A-S Medication Solutions
- 50090-4853 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.
- 62332-009 Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 62332-008 Venlafaxine Hydrochloride 25 mg/1 · Tablet · Alembic Pharmaceuticals Inc.
- 62332-012 Venlafaxine Hydrochloride 100 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