Orange Book product
TYCOLET 500MG;5MG
Orange Book ANDA 089385 · ORTHO MCNEIL PHARMACEUTICAL INC · Discontinued
Key facts
| Proprietary name | TYCOLET |
|---|---|
| Active ingredients | ACETAMINOPHEN, HYDROCODONE BITARTRATE |
| Strength | 500MG;5MG |
| Dosage form | TABLET |
| Route | ORAL |
| Application | ANDA089385 |
| Applicant holder | ORTHO MCNEIL PHARMACEUTICAL INC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Aug 27, 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.