NDC 68382-101 – Venlafaxine
Venlafaxine Hydrochloride 100 mg/1 · Tablet · Oral
Product NDC68382-101
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077653
- Marketed since
- June 13, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 100 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-101-01 | 100 TABLET in 1 BOTTLE (68382-101-01) | Jun 13, 2008 |
| 68382-101-05 | 500 TABLET in 1 BOTTLE (68382-101-05) | Jun 13, 2008 |
| 68382-101-06 | 30 TABLET in 1 BOTTLE (68382-101-06) | Jun 13, 2008 |
| 68382-101-10 | 1000 TABLET in 1 BOTTLE (68382-101-10) | Jun 13, 2008 |
| 68382-101-14 | 60 TABLET in 1 BOTTLE (68382-101-14) | Jun 13, 2008 |
| 68382-101-16 | 90 TABLET in 1 BOTTLE (68382-101-16) | Jun 13, 2008 |
Recalls mentioning this NDC
- D-0310-2025 Apr 16, 2025 · Class II
Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet. - D-202-2013 Apr 3, 2013 · Class II
Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.
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- 46708-431 Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · Alembic Pharmaceuticals Limited
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