NDC 0409-3814 – Morphine Sulfate

Morphine Sulfate .5 mg/mL · Injection, Solution · Epidural, Intrathecal, Intravenous

Human Prescription Drug DEA schedule CII 1 recall

Product NDC0409-3814

Product details

Brand name
Morphine Sulfate
Generic name
Morphine Sulfate
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Epidural, Intrathecal, Intravenous
Marketing category
ANDA · ANDA073509
Marketed since
August 10, 2005
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Morphine Sulfate →

Package NDC codes (1)

Package NDCDescriptionSince
0409-3814-125 VIAL, GLASS in 1 CARTON (0409-3814-12) / 10 mL in 1 VIAL, GLASS (0409-3814-11)Aug 10, 2005

Recalls mentioning this NDC

Other Morphine Sulfate products