NDC 68382-805 – Trazodone Hydrochloride
Trazodone Hydrochloride 50 mg/1 · Tablet · Oral
Product NDC68382-805
Product details
- Brand name
- Trazodone Hydrochloride
- Generic name
- Trazodone Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA205253
- Marketed since
- December 11, 2017
- Marketing end
- December 31, 2028
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Trazodone Hydrochloride 50 mg/1
Uses, dosage, side effects and warnings for Trazodone Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68382-805-01 | 100 TABLET in 1 BOTTLE (68382-805-01) | Dec 11, 2017 |
| 68382-805-05 | 500 TABLET in 1 BOTTLE (68382-805-05) | Dec 11, 2017 |
| 68382-805-06 | 30 TABLET in 1 BOTTLE (68382-805-06) | Dec 11, 2017 |
| 68382-805-10 | 1000 TABLET in 1 BOTTLE (68382-805-10) | Dec 11, 2017 |
| 68382-805-16 | 90 TABLET in 1 BOTTLE (68382-805-16) | Dec 11, 2017 |
| 68382-805-77 | 10 BLISTER PACK in 1 CARTON (68382-805-77) / 10 TABLET in 1 BLISTER PACK (68382-805-30) | Dec 11, 2017 |
Recalls mentioning this NDC
- D-0247-2026 Jan 7, 2026 · Class III
Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.
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