NDC 71335-1752 – Buspirone Hydrochloride
Buspirone Hydrochloride 15 mg/1 · Tablet · Oral
Product NDC71335-1752
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075388
- Marketed since
- July 27, 2020
- 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 |
|---|---|---|
| 71335-1752-1 | 30 TABLET in 1 BOTTLE (71335-1752-1) | Apr 22, 2021 |
| 71335-1752-2 | 100 TABLET in 1 BOTTLE (71335-1752-2) | Dec 31, 2020 |
| 71335-1752-3 | 60 TABLET in 1 BOTTLE (71335-1752-3) | Feb 4, 2021 |
| 71335-1752-4 | 90 TABLET in 1 BOTTLE (71335-1752-4) | Apr 12, 2021 |
| 71335-1752-5 | 120 TABLET in 1 BOTTLE (71335-1752-5) | Dec 10, 2021 |
| 71335-1752-6 | 28 TABLET in 1 BOTTLE (71335-1752-6) | May 3, 2022 |
| 71335-1752-7 | 180 TABLET in 1 BOTTLE (71335-1752-7) | Mar 1, 2022 |
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