NDC 0641-6052 – Meperidine Hydrochloride

Meperidine Hydrochloride 25 mg/mL · Injection · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug DEA schedule CII

Product NDC0641-6052

Product details

Brand name
Meperidine Hydrochloride
Generic name
Meperidine Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA080445
Marketed since
January 22, 1975
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0641-6052-2525 VIAL in 1 CARTON (0641-6052-25) / 1 mL in 1 VIAL (0641-6052-01)Jan 22, 1975

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