NDC 70771-1982 – Cevimeline Hydrochloride

Cevimeline Hydrochloride 30 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC70771-1982

Product details

Brand name
Cevimeline Hydrochloride
Generic name
Cevimeline Hydrochloride
Labeler
Zydus Lifesciences Limited
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA220267
Marketed since
April 15, 2026
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
70771-1982-1100 CAPSULE in 1 BOTTLE (70771-1982-1)Apr 15, 2026

Other Cevimeline hydrochloride products