NDC 71335-9673 – Buspirone Hydrochloride
Buspirone Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-9673
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075388
- Marketed since
- July 27, 2020
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9673-1 | 30 TABLET in 1 BOTTLE (71335-9673-1) | Sep 26, 2023 |
| 71335-9673-2 | 60 TABLET in 1 BOTTLE (71335-9673-2) | Jul 13, 2023 |
| 71335-9673-3 | 90 TABLET in 1 BOTTLE (71335-9673-3) | Mar 20, 2023 |
| 71335-9673-4 | 45 TABLET in 1 BOTTLE (71335-9673-4) | Apr 3, 2024 |
| 71335-9673-5 | 180 TABLET in 1 BOTTLE (71335-9673-5) | Apr 3, 2024 |
| 71335-9673-6 | 120 TABLET in 1 BOTTLE (71335-9673-6) | Apr 3, 2024 |
| 71335-9673-7 | 10 TABLET in 1 BOTTLE (71335-9673-7) | Apr 3, 2024 |
| 71335-9673-8 | 100 TABLET in 1 BOTTLE (71335-9673-8) | Apr 3, 2024 |
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