FDA Orange Book
Generic for Feldene
Feldene contains piroxicam. 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
Yes. The generic name for Feldene is piroxicam. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
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Feldene products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| capsule, oral | 10MG | Marketed (Rx) | AB | 5 | AB |
| capsule, oral | 20MG | Marketed (Rx) | AB | 5 | AB |
NDA 018147, held by PFIZER LABORATORIES DIV PFIZER INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Approved generic piroxicam
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| TEVA PHARMACEUTICALS USA INC | 074131 | AB (A-rated, therapeutically equivalent) | December 11, 1992 | 10MG, 20MG |
| SOLIS PHARMACEUTICALS INC | 074118 | AB (A-rated, therapeutically equivalent) | June 15, 1993 | 10MG, 20MG |
| MICRO LABS LTD | 206152 | AB (A-rated, therapeutically equivalent) | December 29, 2017 | 10MG, 20MG |
| STRIDES PHARMA GLOBAL PTE LTD | 210347 | AB (A-rated, therapeutically equivalent) | January 26, 2018 | 10MG, 20MG |
| ZYDUS LIFESCIENCES LTD | 205585 | AB (A-rated, therapeutically equivalent) | July 17, 2018 | 10MG, 20MG |
Questions
Is there a generic for Feldene?
Yes. The generic name for Feldene is piroxicam. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
What is the generic name for Feldene?
The active ingredient in Feldene is piroxicam, per the FDA Orange Book.
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.