NDC 62135-236 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-236

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA088212
Marketed since
May 26, 1983
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Cyproheptadine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
62135-236-9090 TABLET in 1 BOTTLE (62135-236-90)Jan 5, 2023

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