Buspirone Hydrochloride 71205-0799
Product NDC
71205-0799- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 28, 2002
- Listing Expires
- December 31, 2026
- Application
- ANDA075022
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Buspirone Hydrochloride | 5 mg/1 |
Packaging Options(3)
30 TABLET in 1 BOTTLE (71205-799-30)
60 TABLET in 1 BOTTLE (71205-799-60)
90 TABLET in 1 BOTTLE (71205-799-90)