NDC 71335-2453 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2453

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 (5)

Package NDCDescriptionSince
71335-2453-130 TABLET in 1 BOTTLE (71335-2453-1)Aug 20, 2024
71335-2453-260 TABLET in 1 BOTTLE (71335-2453-2)Aug 20, 2024
71335-2453-328 TABLET in 1 BOTTLE (71335-2453-3)Aug 20, 2024
71335-2453-4100 TABLET in 1 BOTTLE (71335-2453-4)Aug 20, 2024
71335-2453-590 TABLET in 1 BOTTLE (71335-2453-5)Aug 20, 2024

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