Buspirone Hydrochloride 72789-0139
Product NDC
72789-0139- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 27, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA075388
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Buspirone Hydrochloride | 5 mg/1 |
Packaging Options(2)
100 TABLET in 1 BOTTLE, PLASTIC (72789-139-01)
60 TABLET in 1 BOTTLE, PLASTIC (72789-139-60)