Buspirone Hydrochloride
- Product NDC
- 71335-2576
- 11-digit product format
- 713352576
- Labeler code
- 71335
- Product ID
- 71335-2576_57881183-8f81-4e40-8d6b-b73447efe6d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2023-10-17
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 207LT9J9OC | BUSPIRONE HYDROCHLORIDE | 33386-08-2 | BUSPIRONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2576-1 | 71335257601 | 30 TABLET in 1 BOTTLE (71335-2576-1) | 30 tablet | 2025-02-05 | No | No | Historical |
| 71335-2576-2 | 71335257602 | 100 TABLET in 1 BOTTLE (71335-2576-2) | 100 tablet | 2025-02-05 | No | No | Historical |
| 71335-2576-3 | 71335257603 | 60 TABLET in 1 BOTTLE (71335-2576-3) | 60 tablet | 2025-02-05 | No | No | Historical |
| 71335-2576-4 | 71335257604 | 90 TABLET in 1 BOTTLE (71335-2576-4) | 90 tablet | 2025-02-05 | No | No | Historical |
| 71335-2576-5 | 71335257605 | 120 TABLET in 1 BOTTLE (71335-2576-5) | 120 tablet | 2025-02-05 | No | No | Historical |
| 71335-2576-6 | 71335257606 | 28 TABLET in 1 BOTTLE (71335-2576-6) | 28 tablet | 2025-02-05 | No | No | Historical |
| 71335-2576-7 | 71335257607 | 180 TABLET in 1 BOTTLE (71335-2576-7) | 180 tablet | 2025-02-05 | No | No | Historical |