NDC 16729-200 – Buspirone Hydrochloride
Buspirone Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC16729-200
Product details
- Brand name
- Buspirone Hydrochloride
- Generic name
- Buspirone Hydrochloride
- Labeler
- Accord Healthcare Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202557
- Marketed since
- December 15, 2016
- Listing expires
- December 31, 2026
Active ingredients
- Buspirone Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Buspirone hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 16729-200-01 | 100 TABLET in 1 BOTTLE (16729-200-01) | Dec 15, 2016 |
| 16729-200-16 | 500 TABLET in 1 BOTTLE (16729-200-16) | Dec 15, 2016 |
Recalls mentioning this NDC
- D-0375-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0378-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0377-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0376-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection. - D-0379-2023 Mar 8, 2023 · Class II
CGMP Deviations: recalling drug products following an FDA inspection.
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