NDC 71335-2193 – Buspirone Hydrochloride
Buspirone Hydrochloride 7.5 mg/1 · Tablet · Oral
Product NDC71335-2193
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078246
- Marketed since
- February 21, 2020
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 7.5 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2193-1 | 30 TABLET in 1 BOTTLE (71335-2193-1) | Dec 1, 2022 |
| 71335-2193-2 | 90 TABLET in 1 BOTTLE (71335-2193-2) | Dec 1, 2022 |
| 71335-2193-3 | 18 TABLET in 1 BOTTLE (71335-2193-3) | Dec 1, 2022 |
| 71335-2193-4 | 28 TABLET in 1 BOTTLE (71335-2193-4) | Dec 1, 2022 |
| 71335-2193-5 | 60 TABLET in 1 BOTTLE (71335-2193-5) | Dec 1, 2022 |
| 71335-2193-6 | 120 TABLET in 1 BOTTLE (71335-2193-6) | Dec 1, 2022 |
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