NDC 71335-0222 – Buspirone hydrochloride
Buspirone Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-0222
Product details
- Brand name
- Buspirone hydrochloride
- Generic name
- Buspirone hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078888
- Marketed since
- May 3, 2014
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0222-1 | 30 TABLET in 1 BOTTLE (71335-0222-1) | Dec 27, 2021 |
| 71335-0222-2 | 60 TABLET in 1 BOTTLE (71335-0222-2) | Apr 11, 2019 |
| 71335-0222-3 | 90 TABLET in 1 BOTTLE (71335-0222-3) | Dec 27, 2021 |
| 71335-0222-4 | 45 TABLET in 1 BOTTLE (71335-0222-4) | Dec 27, 2021 |
| 71335-0222-5 | 180 TABLET in 1 BOTTLE (71335-0222-5) | Dec 27, 2021 |
| 71335-0222-6 | 120 TABLET in 1 BOTTLE (71335-0222-6) | Dec 27, 2021 |
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