Buspirone Hydrochloride 67046-1352
Product NDC
67046-1352- Manufacturer
- Coupler Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 10, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA078888
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Buspirone Hydrochloride | 7.5 mg/1 |
Packaging Options(1)
30 TABLET in 1 BLISTER PACK (67046-1352-3)