NDC 64980-504 – Cyproheptadine Hydrochloride

Cyproheptadine Hydrochloride 2 mg/5mL · Syrup · Oral

Human Prescription Drug 1 recall

Product NDC64980-504

Product details

Brand name
Cyproheptadine Hydrochloride
Generic name
Cyproheptadine Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Syrup
Route
Oral
Marketing category
ANDA · ANDA040668
Marketed since
July 10, 2006
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
64980-504-48473 mL in 1 BOTTLE (64980-504-48)Jul 10, 2006

Recalls mentioning this NDC

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