NDC 33342-216 – Cevimeline Hydrochloride

Cevimeline Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC33342-216

Product details

Brand name
Cevimeline Hydrochloride
Generic name
Cevimeline Hydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA206808
Marketed since
October 20, 2024
Listing expires
December 31, 2027
Pharmacologic class
Cholinergic Receptor Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
33342-216-11100 CAPSULE in 1 BOTTLE (33342-216-11)Oct 20, 2024

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