NDC 0409-2634 – Hydromorphone Hydrochloride

Hydromorphone Hydrochloride 10 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug DEA schedule CII 3 recalls

Product NDC0409-2634

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA078591
Marketed since
July 31, 2008
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
0409-2634-0110 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-2634-10)Aug 8, 2008
0409-2634-0510 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-05) / 5 mL in 1 VIAL, SINGLE-DOSE (0409-2634-25)Aug 7, 2008
0409-2634-501 VIAL, SINGLE-DOSE in 1 BOX (0409-2634-50) / 50 mL in 1 VIAL, SINGLE-DOSEJul 31, 2008

Recalls mentioning this NDC

Other Hydromorphone Hydrochloride products