NDC 0409-3365 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 2 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug DEA schedule CII 3 recalls

Product NDC0409-3365

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
NDA · NDA200403
Marketed since
December 1, 2011
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0409-3365-1010 VIAL, SINGLE-DOSE in 1 CARTON (0409-3365-10) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-3365-11)Jun 14, 2021

Recalls mentioning this NDC

Other Hydromorphone Hydrochloride products