NDC 71335-2458 – Buspirone Hydrochloride
Buspirone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-2458
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 30 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2458-1 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2458-1) | Aug 20, 2024 |
| 71335-2458-2 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2458-2) | Aug 20, 2024 |
| 71335-2458-3 | 56 TABLET in 1 BOTTLE, PLASTIC (71335-2458-3) | Aug 20, 2024 |
| 71335-2458-4 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2458-4) | Aug 20, 2024 |
| 71335-2458-5 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-2458-5) | Aug 20, 2024 |
| 71335-2458-6 | 15 TABLET in 1 BOTTLE, PLASTIC (71335-2458-6) | Aug 20, 2024 |
| 71335-2458-7 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2458-7) | Aug 20, 2024 |
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