NDC 0703-0113 – Hydromorphone Hydrochloride

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

Human Prescription Drug DEA schedule CII 4 recalls

Product NDC0703-0113

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Teva Parenteral Medicines, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA078591
Marketed since
January 18, 2011
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0703-0113-0310 VIAL in 1 CARTON (0703-0113-03) / 5 mL in 1 VIAL (0703-0113-01)Jan 18, 2011

Recalls mentioning this NDC

Other Hydromorphone Hydrochloride products