NDC 71335-2510 – Buspirone Hydrochloride
Buspirone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-2510
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075022
- Marketed since
- March 26, 2004
- 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 |
|---|---|---|
| 71335-2510-1 | 60 TABLET in 1 BOTTLE (71335-2510-1) | Oct 21, 2024 |
| 71335-2510-2 | 30 TABLET in 1 BOTTLE (71335-2510-2) | Oct 21, 2024 |
| 71335-2510-3 | 56 TABLET in 1 BOTTLE (71335-2510-3) | Oct 21, 2024 |
| 71335-2510-4 | 90 TABLET in 1 BOTTLE (71335-2510-4) | Oct 21, 2024 |
| 71335-2510-5 | 180 TABLET in 1 BOTTLE (71335-2510-5) | Oct 21, 2024 |
| 71335-2510-6 | 15 TABLET in 1 BOTTLE (71335-2510-6) | Oct 21, 2024 |
| 71335-2510-7 | 120 TABLET in 1 BOTTLE (71335-2510-7) | Oct 21, 2024 |
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