NDC 63304-479 – Cevimeline

Cevimeline Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC63304-479

Product details

Brand name
Cevimeline
Generic name
Cevimeline
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
NDA · NDA020989
Marketed since
March 10, 2016
Marketing end
April 30, 2027
Pharmacologic class
Cholinergic Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Cevimeline →

Package NDC codes (1)

Package NDCDescriptionSince
63304-479-01100 CAPSULE in 1 BOTTLE (63304-479-01)Mar 10, 2016

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