NDC 71335-1107 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1107

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209172
Marketed since
April 11, 2018
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71335-1107-130 TABLET in 1 BOTTLE (71335-1107-1)Feb 21, 2019
71335-1107-260 TABLET in 1 BOTTLE (71335-1107-2)Feb 21, 2019
71335-1107-328 TABLET in 1 BOTTLE (71335-1107-3)Feb 21, 2019
71335-1107-4100 TABLET in 1 BOTTLE (71335-1107-4)Feb 21, 2019
71335-1107-590 TABLET in 1 BOTTLE (71335-1107-5)Feb 21, 2019

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