FDA Orange Book
Is there a generic for Clenpiq?
Clenpiq contains citric acid, magnesium oxide and sodium picosulfate. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.
Source: FDA Orange Book data file dated 2026-10-09. Publisher page
No. The Orange Book lists no active FDA-approved generic (ANDA) for Clenpiq (citric acid, magnesium oxide and sodium picosulfate). The Orange Book shows its last listed patent expires January 27, 2038.
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Clenpiq products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| solution, oral | 12GM/BOT;3.5GM/BOT;10MG/BOT | Marketed (Rx) | None | 0 | None |
NDA 209589, held by FERRING PHARMACEUTICALS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Clenpiq patents
| Patent | Expires | Covers | Use code | NDA |
|---|---|---|---|---|
| 11191753 | June 23, 2034 | Method of use | U-3261 | 209589 |
| 12576072 | June 23, 2034 | Drug product | U-3261 | 209589 |
| 10624879 | June 23, 2034 | Drug product | None | 209589 |
| 9827231 | June 26, 2034 | Drug product | U-2162 | 209589 |
| 12458634 | January 27, 2038 | Drug product | None | 209589 |
Clenpiq NDC codes
Questions
Is there a generic for Clenpiq?
No. The Orange Book lists no active FDA-approved generic (ANDA) for Clenpiq (citric acid, magnesium oxide and sodium picosulfate). The Orange Book shows its last listed patent expires January 27, 2038.
What is the generic name for Clenpiq?
The active ingredient in Clenpiq is citric acid, magnesium oxide and sodium picosulfate, per the FDA Orange Book.
When does the Clenpiq patent expire?
The last patent listed for Clenpiq in the Orange Book expires January 27, 2038. A listed patent expiry date is not a generic launch date.
What does a therapeutic equivalence code mean?
In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.