NDC 71335-2576 – Buspirone Hydrochloride
Buspirone Hydrochloride 15 mg/1 · Tablet · Oral
Product NDC71335-2576
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210907
- Marketed since
- October 17, 2023
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 15 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2576-1 | 30 TABLET in 1 BOTTLE (71335-2576-1) | Feb 5, 2025 |
| 71335-2576-2 | 100 TABLET in 1 BOTTLE (71335-2576-2) | Feb 5, 2025 |
| 71335-2576-3 | 60 TABLET in 1 BOTTLE (71335-2576-3) | Feb 5, 2025 |
| 71335-2576-4 | 90 TABLET in 1 BOTTLE (71335-2576-4) | Feb 5, 2025 |
| 71335-2576-5 | 120 TABLET in 1 BOTTLE (71335-2576-5) | Feb 5, 2025 |
| 71335-2576-6 | 28 TABLET in 1 BOTTLE (71335-2576-6) | Feb 5, 2025 |
| 71335-2576-7 | 180 TABLET in 1 BOTTLE (71335-2576-7) | Feb 5, 2025 |
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