NDC 72516-024 – Papaverine Hydrochloride

Papaverine Hydrochloride 30 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC72516-024

Product details

Brand name
Papaverine Hydrochloride
Generic name
Papaverine Hydrochloride
Labeler
Oryza Pharmaceuticals Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
February 1, 2021
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72516-024-1010 VIAL in 1 CARTON (72516-024-10) / 2 mL in 1 VIALFeb 1, 2021
72516-024-2525 VIAL in 1 CARTON (72516-024-25) / 2 mL in 1 VIALFeb 1, 2021

Recalls mentioning this NDC

Other Papaverine Hydrochloride products