NDC 63323-614 – Hydralazine Hydrochloride

Hydralazine Hydrochloride 20 mg/mL · Injection · Intramuscular, Intravenous

Human Prescription Drug 2 recalls

Product NDC63323-614

Product details

Brand name
Hydralazine Hydrochloride
Generic name
Hydralazine Hydrochloride
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection
Route
Intramuscular, Intravenous
Marketing category
ANDA · ANDA040388
Marketed since
September 5, 2001
Listing expires
December 31, 2026
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
63323-614-0125 VIAL, SINGLE-DOSE in 1 CARTON (63323-614-01) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-00)Sep 5, 2001
63323-614-0625 VIAL, SINGLE-DOSE in 1 CARTON (63323-614-06) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-03)Sep 5, 2001
63323-614-1625 VIAL, SINGLE-USE in 1 TRAY (63323-614-16) / 1 mL in 1 VIAL, SINGLE-USE (63323-614-41)Sep 5, 2001
63323-614-5525 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) / 1 mL in 1 VIAL, SINGLE-DOSE (63323-614-21)Jan 31, 2011

Recalls mentioning this NDC

Other Hydralazine Hydrochloride products