Clonidine Hydrochloride 58657-0649
Product NDC
58657-0649- Manufacturer
- Method Pharmaceuticals, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA202297
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Clonidine Hydrochloride | .3 mg/1 |
Drug Class
Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE (58657-649-01)
1000 TABLET in 1 BOTTLE (58657-649-10)
500 TABLET in 1 BOTTLE (58657-649-50)