Orange Book product
NALOXONE 0.02MG/ML
Orange Book ANDA 070189 · WYETH AYERST LABORATORIES · Discontinued
Key facts
| Proprietary name | NALOXONE |
|---|---|
| Active ingredients | NALOXONE HYDROCHLORIDE |
| Strength | 0.02MG/ML |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA070189 |
| Applicant holder | WYETH AYERST LABORATORIES |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Sep 24, 1986 |
At a glance
- None 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.