Buspirone Hcl
- Product NDC
- 72189-235
- 11-digit product format
- 721890235
- Labeler code
- 72189
- Product ID
- 72189-235_2c2865d6-1e65-7250-e063-6394a90a6128
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Buspirone Hcl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct Rx
- Application
- ANDA210907
- Marketing category
- ANDA
- Marketing start
- 2022-03-16
- 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 |
|---|
| 72189-235-30 | 72189023530 | 30 TABLET in 1 BOTTLE (72189-235-30) | 30 tablet | 2022-03-16 | No | No | Historical |
| 72189-235-60 | 72189023560 | 60 TABLET in 1 BOTTLE (72189-235-60) | 60 tablet | 2022-03-16 | No | No | Historical |
| 72189-235-90 | 72189023590 | 90 TABLET in 1 BOTTLE (72189-235-90) | 90 tablet | 2022-03-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Buspirone Hcl | Direct Rx | 2025-01-20 | HUMAN PRESCRIPTION DRUG LABEL | 5 |