NDC 71335-2237 – Buspirone hydrochloride
Buspirone Hydrochloride 7.5 mg/1 · Tablet · Oral
Product NDC71335-2237
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
- March 21, 2023
- 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 |
|---|---|---|
| 71335-2237-1 | 30 TABLET in 1 BOTTLE (71335-2237-1) | Apr 3, 2024 |
| 71335-2237-2 | 90 TABLET in 1 BOTTLE (71335-2237-2) | Aug 29, 2023 |
| 71335-2237-3 | 18 TABLET in 1 BOTTLE (71335-2237-3) | Apr 3, 2024 |
| 71335-2237-4 | 28 TABLET in 1 BOTTLE (71335-2237-4) | Apr 3, 2024 |
| 71335-2237-5 | 60 TABLET in 1 BOTTLE (71335-2237-5) | Apr 3, 2024 |
| 71335-2237-6 | 120 TABLET in 1 BOTTLE (71335-2237-6) | Apr 3, 2024 |
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