NDC 16571-657 – Cevimeline Hydrochloride

Cevimeline Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC16571-657

Product details

Brand name
Cevimeline Hydrochloride
Generic name
Cevimeline Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA203775
Marketed since
June 17, 2014
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Receptor Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
16571-657-10100 CAPSULE in 1 BOTTLE (16571-657-10)Jun 17, 2014

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