NDC 71335-2060 – Buspirone Hydrochloride
Buspirone Hydrochloride 15 mg/1 · Tablet · Oral
Product NDC71335-2060
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 15 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2060-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2060-1) | Mar 23, 2022 |
| 71335-2060-2 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2060-2) | Apr 3, 2024 |
| 71335-2060-3 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2060-3) | Mar 7, 2022 |
| 71335-2060-4 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2060-4) | Feb 1, 2023 |
| 71335-2060-5 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2060-5) | Feb 2, 2023 |
| 71335-2060-6 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-2060-6) | Apr 3, 2024 |
| 71335-2060-7 | 180 TABLET in 1 BOTTLE, PLASTIC (71335-2060-7) | Apr 3, 2024 |
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