NDC 50268-201 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50268-201

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040537
Marketed since
October 30, 2025
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
50268-201-1550 BLISTER PACK in 1 BOX (50268-201-15) / 1 TABLET in 1 BLISTER PACK (50268-201-11)Oct 30, 2025

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