NDC 71209-088 – Venlafaxine
Venlafaxine Hydrochloride 150 mg/1 · Tablet, Coated · Oral
Product NDC71209-088
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Cadila Pharmaceuticals Limited
- 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 150 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71209-088-01 | 30 TABLET, COATED in 1 BOTTLE (71209-088-01) | Aug 16, 2018 |
| 71209-088-04 | 90 TABLET, COATED in 1 BOTTLE (71209-088-04) | Aug 16, 2018 |
| 71209-088-11 | 1000 TABLET, COATED in 1 BOTTLE (71209-088-11) | Aug 16, 2018 |
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- 27241-224 Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Ajanta Pharma USA Inc.