NDC 0641-2341 – Hydromorphone Hydrochloride

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

Human Prescription Drug DEA schedule CII

Product NDC0641-2341

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
January 1, 1972
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
0641-2341-4120 VIAL in 1 CARTON (0641-2341-41) / 20 mL in 1 VIAL (0641-2341-39)Jan 1, 1972

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