Guanfacine 70518-4675
Product NDC
70518-4675- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 2, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA219033
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Guanfacine Hydrochloride | 2 mg/1 |
Drug Class
Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]
Packaging Options(1)
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4675-0)