Buspirone Hydrochloride 00904-7122
Product NDC
00904-7122- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 29, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA204582
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Buspirone Hydrochloride | 5 mg/1 |
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (0904-7122-61) / 1 TABLET in 1 BLISTER PACK