NDC 0641-6151 – Hydromorphone Hydrochloride

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

Human Prescription Drug DEA schedule CII

Product NDC0641-6151

Product details

Brand name
Hydromorphone Hydrochloride
Generic name
Hydromorphone Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA202159
Marketed since
July 1, 2018
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
0641-6151-2525 VIAL, SINGLE-DOSE in 1 CARTON (0641-6151-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6151-01)Jul 1, 2018

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