BUSPIRONE HYDROCHLORIDE
- Product NDC
- 71335-2073
- 11-digit product format
- 713352073
- Labeler code
- 71335
- Product ID
- 71335-2073_8c0eb390-f204-4192-969b-63983212a817
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUSPIRONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078246
- Marketing category
- ANDA
- Marketing start
- 2020-02-21
- 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 |
|---|
| 71335-2073-1 | 71335207301 | 30 TABLET in 1 BOTTLE (71335-2073-1) | 30 tablet | 2022-04-25 | No | No | Historical |
| 71335-2073-2 | 71335207302 | 100 TABLET in 1 BOTTLE (71335-2073-2) | 100 tablet | 2022-04-25 | No | No | Historical |
| 71335-2073-3 | 71335207303 | 60 TABLET in 1 BOTTLE (71335-2073-3) | 60 tablet | 2022-04-25 | No | No | Historical |
| 71335-2073-4 | 71335207304 | 90 TABLET in 1 BOTTLE (71335-2073-4) | 90 tablet | 2022-04-25 | No | No | Historical |
| 71335-2073-5 | 71335207305 | 120 TABLET in 1 BOTTLE (71335-2073-5) | 120 tablet | 2022-04-25 | No | No | Historical |
| 71335-2073-6 | 71335207306 | 28 TABLET in 1 BOTTLE (71335-2073-6) | 28 tablet | 2022-04-25 | No | No | Historical |
| 71335-2073-7 | 71335207307 | 180 TABLET in 1 BOTTLE (71335-2073-7) | 180 tablet | 2022-04-25 | No | No | Historical |