Buspirone hydrochloride
- Product NDC
- 71335-2820
- 11-digit product format
- 713352820
- Labeler code
- 71335
- Product ID
- 71335-2820_2dcf0b87-6917-4c75-ae93-c27bf9344c12
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078888
- Marketing category
- ANDA
- Marketing start
- 2023-03-21
- Substance
- BUSPIRONE HYDROCHLORIDE
- Active strength
- 7.5 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 |
|---|
| 71335-2820-1 | 71335282001 | 100 TABLET in 1 BOTTLE (71335-2820-1) | 100 tablet | 2025-11-10 | No | No | Historical |