NDC 43386-999 – Cevimeline hydrochloride

Cevimeline Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC43386-999

Product details

Brand name
Cevimeline hydrochloride
Generic name
Cevimeline hydrochloride
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA204746
Marketed since
December 30, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Receptor Agonist

Active ingredients

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

Package NDC codes (0)

Package NDCDescriptionSince

Other Cevimeline hydrochloride products