NDC 71335-2964 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2964

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212491
Marketed since
February 24, 2021
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
71335-2964-190 TABLET in 1 BOTTLE (71335-2964-1)Nov 10, 2025

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