NDC 50742-190 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50742-190

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Ingenus Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA205087
Marketed since
September 23, 2015
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
50742-190-01100 TABLET in 1 BOTTLE, PLASTIC (50742-190-01)Sep 23, 2015
50742-190-101000 TABLET in 1 BOTTLE, PLASTIC (50742-190-10)Sep 23, 2015

Other Cyproheptadine Hydrochloride products