NDC 63629-7046 – Nefazodone Hydrochloride
Nefazodone Hydrochloride 150 mg/1 · Tablet · Oral
Product NDC63629-7046
Product details
- Brand name
- Nefazodone Hydrochloride
- Generic name
- Nefazodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076037
- Marketed since
- September 16, 2003
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Nefazodone Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Nefazodone Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 63629-7046-1 | 30 TABLET in 1 BOTTLE (63629-7046-1) | Feb 8, 2022 |
| 63629-7046-2 | 120 TABLET in 1 BOTTLE (63629-7046-2) | Oct 18, 2016 |
| 63629-7046-3 | 28 TABLET in 1 BOTTLE (63629-7046-3) | Feb 8, 2022 |
| 63629-7046-4 | 60 TABLET in 1 BOTTLE (63629-7046-4) | Feb 8, 2022 |
Other Nefazodone Hydrochloride products
- 0093-1024 Nefazodone Hydrochloride 100 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.
- 0093-1025 Nefazodone Hydrochloride 200 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.
- 0093-1026 Nefazodone Hydrochloride 250 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.
- 0093-7113 Nefazodone Hydrochloride 150 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.
- 0093-7178 Nefazodone Hydrochloride 50 mg/1 · Tablet · Teva Pharmaceuticals USA, Inc.