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DESIPRAMINE HYDROCHLORIDE — FDA application ANDA205153

Application ANDA205153 · type ANDA · FDA status: approved · original approval 2016-10-28

Listed sponsor: ANI PHARMS · ANIP 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
001DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLETORAL10MGDiscontinuednot listedNo
002DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLETORAL25MGDiscontinuednot listedNo
003DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLETORAL50MGDiscontinuednot listedNo
004DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLETORAL75MGDiscontinuednot listedNo
005DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLETORAL100MGDiscontinuednot listedNo
006DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLETORAL150MGDiscontinuednot listedNo

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

No Orange Book patent or exclusivity listings joined to this application.

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.