NDC 71335-1924 – Buspirone Hydrochloride
Buspirone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC71335-1924
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210907
- Marketed since
- November 14, 2019
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1924-1 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-1924-1) | Aug 12, 2021 |
| 71335-1924-2 | 45 TABLET in 1 BOTTLE, PLASTIC (71335-1924-2) | Oct 19, 2022 |
| 71335-1924-3 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-1924-3) | Dec 13, 2021 |
| 71335-1924-4 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-1924-4) | Nov 29, 2021 |
| 71335-1924-5 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-1924-5) | Apr 5, 2024 |
| 71335-1924-6 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-1924-6) | Apr 5, 2024 |
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