NDC 71335-0007 – Buspirone Hydrochloride
Buspirone Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-0007
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202557
- Marketed since
- December 15, 2016
- Listing expires
- December 31, 2027
Active ingredients
- Buspirone Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0007-1 | 30 TABLET in 1 BOTTLE (71335-0007-1) | May 14, 2026 |
| 71335-0007-2 | 60 TABLET in 1 BOTTLE (71335-0007-2) | May 14, 2026 |
| 71335-0007-3 | 90 TABLET in 1 BOTTLE (71335-0007-3) | May 14, 2026 |
| 71335-0007-4 | 45 TABLET in 1 BOTTLE (71335-0007-4) | May 14, 2026 |
| 71335-0007-5 | 180 TABLET in 1 BOTTLE (71335-0007-5) | May 14, 2026 |
| 71335-0007-6 | 120 TABLET in 1 BOTTLE (71335-0007-6) | May 14, 2026 |
| 71335-0007-7 | 10 TABLET in 1 BOTTLE (71335-0007-7) | May 14, 2026 |
| 71335-0007-8 | 100 TABLET in 1 BOTTLE (71335-0007-8) | May 14, 2026 |
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