NDC 70436-041 – Guanfacine

Guanfacine Hydrochloride 3 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC70436-041

Product details

Brand name
Guanfacine
Generic name
Guanfacine
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA213428
Marketed since
August 1, 2022
Listing expires
December 31, 2026
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Guanfacine →

Package NDC codes (1)

Package NDCDescriptionSince
70436-041-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-041-01)Aug 1, 2022

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