NDC 70518-4667 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4667

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040537
Marketed since
May 27, 2026
Listing expires
December 31, 2027

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-4667-050 POUCH in 1 BOX (70518-4667-0) / 1 TABLET in 1 POUCH (70518-4667-1)May 27, 2026

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