NDC 70069-672 – Nalbuphine hydrochloride

Nalbuphine Hydrochloride 20 mg/mL · Injection · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug

Product NDC70069-672

Product details

Brand name
Nalbuphine hydrochloride
Generic name
Nalbuphine hydrochloride
Labeler
Somerset Therapeutics, LLC
Dosage form
Injection
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA216050
Marketed since
September 25, 2024
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist/Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Nalbuphine hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
70069-672-1010 AMPULE in 1 CARTON (70069-672-10) / 1 mL in 1 AMPULE (70069-672-01)Sep 25, 2024

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