NDC 33342-195 – Venlafaxine hydrochloride
Venlafaxine Hydrochloride 75 mg/1 · Capsule, Extended Release · Oral
Product NDC33342-195
Product details
- Brand name
- Venlafaxine hydrochloride
- Generic name
- Venlafaxine hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204889
- Marketed since
- October 6, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 75 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 33342-195-07 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-07) | Oct 6, 2017 |
| 33342-195-10 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-10) | Aug 14, 2018 |
| 33342-195-11 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-11) | Aug 14, 2018 |
| 33342-195-15 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-195-15) | Oct 6, 2017 |
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