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PRAVIGARD PAC (COPACKAGED) — FDA application NDA021387

Application NDA021387 · type NDA · FDA status: approved · original approval 2003-06-24

Listed sponsor: BRISTOL MYERS SQUIBB · BMY 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
001PRAVIGARD PAC (COPACKAGED)ASPIRIN; PRAVASTATIN SODIUMTABLETORAL81MG;20MGDiscontinuednot listedNo
002PRAVIGARD PAC (COPACKAGED)ASPIRIN; PRAVASTATIN SODIUMTABLETORAL81MG;40MGDiscontinuednot listedNo
003PRAVIGARD PAC (COPACKAGED)ASPIRIN; PRAVASTATIN SODIUMTABLETORAL81MG;80MGDiscontinuednot listedNo
004PRAVIGARD PAC (COPACKAGED)ASPIRIN; PRAVASTATIN SODIUMTABLETORAL325MG;20MGDiscontinuednot listedNo
005PRAVIGARD PAC (COPACKAGED)ASPIRIN; PRAVASTATIN SODIUMTABLETORAL325MG;40MGDiscontinuednot listedNo
006PRAVIGARD PAC (COPACKAGED)ASPIRIN; PRAVASTATIN SODIUMTABLETORAL325MG;80MGDiscontinuednot 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: Large-cap biopharma

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.