Orange Book product

NALBUPHINE HYDROCHLORIDE 20MG/ML (20MG/ML)

Orange Book ANDA 072075 · IGI LABORATORIES INC · Discontinued

Key facts

Proprietary name NALBUPHINE HYDROCHLORIDE
Active ingredients NALBUPHINE HYDROCHLORIDE
Strength 20MG/ML (20MG/ML)
Dosage form SOLUTION
Route INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Application ANDA072075
Applicant holder IGI LABORATORIES INC
Marketing status Discontinued
Reference listed drug (RLD) No
Reference standard (RS) No
Approval date Apr 10, 1989

At a glance

  • 1–9 Marketed products with the same ingredient, strength and form
  • 1–9 Products in this application
  • No Reference listed drug

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Orange Book products

The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.

Source: U.S. Food and Drug Administration (FDA), Approved Drug Products with Therapeutic Equivalence Evaluations (Orange Book)

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