NDC 72241-077 – Venlafaxine
Venlafaxine Hydrochloride 225 mg/1 · Tablet, Coated · Oral
Product NDC72241-077
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Modavar Pharmaceuticals LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211323
- Marketed since
- January 5, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 225 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 72241-077-04 | 90 TABLET, COATED in 1 BOTTLE (72241-077-04) | Aug 16, 2018 |
| 72241-077-11 | 1000 TABLET, COATED in 1 BOTTLE (72241-077-11) | Aug 16, 2018 |
| 72241-077-22 | 30 TABLET, COATED in 1 BOTTLE (72241-077-22) | Aug 16, 2018 |
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