Orange Book product
NANDROLONE PHENPROPIONATE 25MG/ML
Orange Book ANDA 086386 · WATSON LABORATORIES INC · Discontinued
Key facts
| Proprietary name | NANDROLONE PHENPROPIONATE |
|---|---|
| Active ingredients | NANDROLONE PHENPROPIONATE |
| Strength | 25MG/ML |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Application | ANDA086386 |
| Applicant holder | WATSON LABORATORIES INC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jun 17, 1983 |
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.