NDC 71335-2264 – Cevimeline Hydrochloride

Cevimeline Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-2264

Product details

Brand name
Cevimeline Hydrochloride
Generic name
Cevimeline Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA091591
Marketed since
July 8, 2013
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Cevimeline hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2264-130 CAPSULE in 1 BOTTLE (71335-2264-1)Oct 27, 2023
71335-2264-260 CAPSULE in 1 BOTTLE (71335-2264-2)Oct 27, 2023
71335-2264-390 CAPSULE in 1 BOTTLE (71335-2264-3)Oct 27, 2023

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