grepcent public filings, reorganized for comparison

XPHOZAH — FDA application NDA213931

Application NDA213931 · type NDA · FDA status: approved · original approval 2023-10-17

Listed sponsor: ARDELYX INC · ARDX company profile · exact_unique

Sponsor as listed in Drugs@FDA at retrieval (2026-08-07); FDA sponsor listings can lag ownership transfers.

FDA application facts

ProductFDA-listed trade nameActive ingredientDosage formRouteStrengthMarketing statusTE codeRLD
001XPHOZAHTENAPANOR HYDROCHLORIDETABLETORALEQ 10MG BASEDiscontinuednot listedYes
002XPHOZAHTENAPANOR HYDROCHLORIDETABLETORALEQ 20MG BASEPrescriptionnot listedYes
003XPHOZAHTENAPANOR HYDROCHLORIDETABLETORALEQ 30MG BASEPrescriptionnot listedYes

Product, form, strength, reference-drug and marketing-status fields: Drugs@FDA data files; TE and RLD fields: Orange Book data files. Retrieved 2026-08-07.

Orange Book patent and exclusivity listings

ListingProductDescriptive dateFlags/code
Patent 12016856001listed patent expiry date: 2029-12-30drug substance, drug product
Patent 12016856002listed patent expiry date: 2029-12-30drug substance, drug product
Patent 12016856003listed patent expiry date: 2029-12-30drug substance, drug product
Patent 8969377001listed patent expiry date: 2029-12-30drug substance, drug product
Patent 8969377002listed patent expiry date: 2029-12-30drug substance, drug product
Patent 8969377003listed patent expiry date: 2029-12-30drug substance, drug product
Patent 8541448001listed patent expiry date: 2033-08-01drug substance, drug product
Patent 8541448002listed patent expiry date: 2033-08-01drug substance, drug product
Patent 8541448003listed patent expiry date: 2033-08-01drug substance, drug product
Patent 10272079001listed patent expiry date: 2034-04-10U-381
Patent 10272079001listed patent expiry date: 2034-04-10U-3736
Patent 10272079002listed patent expiry date: 2034-04-10U-3736
Patent 10272079002listed patent expiry date: 2034-04-10U-381
Patent 10272079003listed patent expiry date: 2034-04-10U-3736
Patent 10272079003listed patent expiry date: 2034-04-10U-381
Patent 10940146001listed patent expiry date: 2034-04-10U-381
Patent 10940146001listed patent expiry date: 2034-04-10U-3736
Patent 10940146002listed patent expiry date: 2034-04-10U-3736
Patent 10940146002listed patent expiry date: 2034-04-10U-381
Patent 10940146003listed patent expiry date: 2034-04-10U-3736
Patent 10940146003listed patent expiry date: 2034-04-10U-381
Patent 12539299001listed patent expiry date: 2042-11-26drug product
Patent 12539299002listed patent expiry date: 2042-11-26drug product
Patent 12539299003listed patent expiry date: 2042-11-26drug product
Exclusivity NP001listed exclusivity date: 2026-10-17FDA code as listed
Exclusivity NP002listed exclusivity date: 2026-10-17FDA code as listed
Exclusivity NP003listed exclusivity date: 2026-10-17FDA code as listed
NDA213931 FDA listing dates. Source: Drugs@FDA and FDA Orange Book.NDA213931 FDA listing dates. Source: Drugs@FDA and FDA Orange Book.NDA213931 FDA listing datesDescriptive regulatory dates only; no relationship to revenue or future sales is stated or implied.Source: Drugs@FDA and FDA Orange Book.Listed dateDated listing marker0.001.002.002023-10-171.002026-10-171.002029-12-301.002033-08-011.002034-04-101.002042-11-261.00

Patent and exclusivity dates are regulatory listings from the FDA Orange Book; no relationship to revenue or future sales is stated or implied.

Compound cross-links

Ingredient–compound links use FDA openFDA/GSRS identifiers and an exact lmmol InChIKey join. Ingredient names cannot create a link.

Related pages

Sponsor company · FDA-approved application index

Peer clusters: No published peer-cluster link for this sponsor.

Sources: Drugs@FDA · Orange Book · openFDA application record. FDA data retrieved 2026-08-07.

Regulatory listing data as published by FDA; not medical or investment advice.