Orange Book product
CODRIX 500MG;30MG
Orange Book ANDA 040441 · WATSON LABORATORIES INC FLORIDA · Discontinued
Key facts
| Proprietary name | CODRIX |
|---|---|
| Active ingredients | ACETAMINOPHEN, CODEINE PHOSPHATE |
| Strength | 500MG;30MG |
| Dosage form | TABLET |
| Route | ORAL |
| Application | ANDA040441 |
| Applicant holder | WATSON LABORATORIES INC FLORIDA |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Mar 27, 2003 |
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.