NDC 68001-158 – Venlafaxine
Venlafaxine Hydrochloride 37.5 mg/1 · Tablet · Oral
Product NDC68001-158
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 37.5 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68001-158-00 | 100 TABLET in 1 BOTTLE (68001-158-00) | Nov 25, 2013 |
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