NDC 72162-2066 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-2066

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 (4)

Package NDCDescriptionSince
72162-2066-01000 TABLET in 1 BOTTLE (72162-2066-0)Aug 15, 2023
72162-2066-1100 TABLET in 1 BOTTLE (72162-2066-1)Aug 15, 2023
72162-2066-2120 TABLET in 1 BOTTLE (72162-2066-2)Aug 15, 2023
72162-2066-990 TABLET in 1 BOTTLE (72162-2066-9)Aug 15, 2023

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