Guanfacine 63304-0924
Product NDC
63304-0924- Manufacturer
- Sun Pharmaceutical Industries, Inc
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 17, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA205689
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Guanfacine Hydrochloride | 1 mg/1 |
Drug Class
Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]
Packaging Options(3)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-924-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-924-05)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-924-30)