Guanfacine 70436-0041-01

Package NDC

70436-0041-01

Manufacturer: Slate Run Pharmaceuticals, Llc
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 1, 2022
Listing Expires: December 31, 2026
Application: ANDA213428

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Active Ingredients

Ingredient	Strength
Guanfacine Hydrochloride	3 mg/1

Drug Class

Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]

Selected Package

70436-0041-01Selected

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-041-01)