NDC 71335-1749 – Buspirone Hydrochloride
Buspirone Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC71335-1749
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 30 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1749-1 | 60 TABLET in 1 BOTTLE (71335-1749-1) | Aug 10, 2021 |
| 71335-1749-2 | 30 TABLET in 1 BOTTLE (71335-1749-2) | Jun 4, 2021 |
| 71335-1749-3 | 56 TABLET in 1 BOTTLE (71335-1749-3) | Apr 12, 2021 |
| 71335-1749-4 | 90 TABLET in 1 BOTTLE (71335-1749-4) | Jan 19, 2022 |
| 71335-1749-5 | 180 TABLET in 1 BOTTLE (71335-1749-5) | Jan 31, 2022 |
| 71335-1749-6 | 15 TABLET in 1 BOTTLE (71335-1749-6) | Jan 21, 2021 |
| 71335-1749-7 | 120 TABLET in 1 BOTTLE (71335-1749-7) | Dec 10, 2021 |
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