NDC 0615-7714 – Buspirone Hydrochloride
Buspirone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC0615-7714
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075022
- Marketed since
- February 28, 2002
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 0615-7714-05 | 15 TABLET in 1 BLISTER PACK (0615-7714-05) | Nov 21, 2022 |
| 0615-7714-30 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7714-30) / 5 TABLET in 1 BLISTER PACK | Apr 23, 2012 |
| 0615-7714-39 | 30 TABLET in 1 BLISTER PACK (0615-7714-39) | Apr 23, 2012 |
Recalls mentioning this NDC
- D-0113-2024 Nov 29, 2023 · Class III
Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots - D-0114-2024 Nov 29, 2023 · Class III
Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots
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