Orange Book product
ULTRACEF EQ 125MG BASE/5ML
Orange Book ANDA 062376 · BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO · Discontinued
Key facts
| Proprietary name | ULTRACEF |
|---|---|
| Active ingredients | CEFADROXIL/CEFADROXIL HEMIHYDRATE |
| Strength | EQ 125MG BASE/5ML |
| Dosage form | FOR SUSPENSION |
| Route | ORAL |
| Application | ANDA062376 |
| Applicant holder | BRISTOL LABORATORIES INC DIV BRISTOL MYERS CO |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Mar 16, 1982 |
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.