NDC 70710-1110 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-1110

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208938
Marketed since
July 20, 2017
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70710-1110-01000 TABLET in 1 BOTTLE (70710-1110-0)Jul 20, 2017
70710-1110-1100 TABLET in 1 BOTTLE (70710-1110-1)Jul 20, 2017

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