Orange Book product
NALOXONE HYDROCHLORIDE 0.4MG/ML
Orange Book ANDA 208872 · RISING PHARMA HOLDINGS INC · Prescription
Key facts
| Proprietary name | NALOXONE HYDROCHLORIDE |
|---|---|
| Active ingredients | NALOXONE HYDROCHLORIDE |
| Strength | 0.4MG/ML |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA208872 |
| Applicant holder | RISING PHARMA HOLDINGS INC |
| Marketing status | Prescription |
| Therapeutic equivalence (TE) code | AP |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Mar 14, 2017 |
At a glance
- 10–99 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.