Buspirone Hydrochloride 00093-5200
Product NDC
00093-5200- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 26, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA075022
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Buspirone Hydrochloride | 30 mg/1 |
Packaging Options(2)
500 TABLET in 1 BOTTLE (0093-5200-05)
60 TABLET in 1 BOTTLE (0093-5200-06)