NDC 57664-392 – Venlafaxine
Venlafaxine Hydrochloride 25 mg/1 · Tablet · Oral
Product NDC57664-392
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078627
- Marketed since
- June 13, 2008
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 57664-392-88 | 100 TABLET in 1 BOTTLE (57664-392-88) | Jun 13, 2008 |
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