Orange Book product
NALBUPHINE HYDROCHLORIDE 20MG/ML (20MG/ML)
Orange Book ANDA 070917 · ABBOTT LABORATORIES HOSP PRODUCTS DIV · Discontinued
Key facts
| Proprietary name | NALBUPHINE HYDROCHLORIDE |
|---|---|
| Active ingredients | NALBUPHINE HYDROCHLORIDE |
| Strength | 20MG/ML (20MG/ML) |
| Dosage form | SOLUTION |
| Route | INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
| Application | ANDA070917 |
| Applicant holder | ABBOTT LABORATORIES HOSP PRODUCTS DIV |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Feb 3, 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.