Market LIVE
Published markets; coverage varies by country
Product profile · United States

GADAVIST

 ·  Patent Litigation & Settlement History ↓

IngredientGADOBUTROL
Application typeNDA
Application201277
Product003
Dosage formSOLUTION
RouteINTRAVENOUS
Strength9.0708GM/15ML (604.72MG/ML)
Approval date2011-03-14
Marketing statusPrescription
Status event—
ApplicantBAYER HLTHCARE
Product source

Current GenericRadar decision

Year2011
SelectionEXCLUDED
ReviewFINAL
Anchor typePRODUCT_APPROVAL
Anchor date2011-03-14
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA—
Status event—

MRI/MRA contrast agent; gadobutrol for CNS, breast, vascular and cardiac diagnostic imaging.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
No patent facts are recorded for this product.

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
No exclusivity facts are recorded in this product snapshot.

2026-10-10 · NO_RECORD_IN_CURRENT_SNAPSHOT · Historical coverage: NOT_COMPLETE

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
215061 / 004APPLICATION_FINAL_OBSERVATION · FINAL_PRODUCT_DATE_UNVERIFIED——HENGRUI PHARMANEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
216081 / 006FINAL_APPROVAL · FINAL_APPROVED2022-11-17—JIANGSU HENGRUI PHARMACEUTICALS CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217480 / 002FINAL_APPROVAL · FINAL_APPROVED2023-03-15—HAINAN POLY PHARMACEUTICAL CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219146 / 004FINAL_APPROVAL · FINAL_APPROVED2026-06-08—ZENARA PHARMA PRIVATE LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
219287 / 003FINAL_APPROVAL · FINAL_APPROVED2026-06-11—VIWIT PHARMACEUTICAL CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215957 / 004FINAL_APPROVAL · FINAL_APPROVED2026-06-29—GE HEALTHCARE INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource

Market Entry Information

API filings, authorized generics and linked regulatory milestones.

API Master Files & Certifications 0 records

Ingredient-level registrations from linked public manufacturer portfolios. A filing does not establish supply to this finished product. DMFs are not FDA approvals.

APIHolder / manufacturerHolder countryFiling typeNumberStatusFiled dateAvailable for referenceSourceLast verified
No master-file or certification records are linked through public manufacturer portfolios.

Authorized Generics 0 records

Authorized generics are shown separately from independent ANDA approvals.

Application / productApplicantEvent / status First marketed Product mappingSourceLast verified
No authorized-generic records are linked to this product.

Tentative ANDA Approvals 0 records

Tentative approval is not final approval. Historical tentative approvals remain visible after a linked final approval.

Application / productApplicantEvent / status Tentative date Follow-up final approvalProduct mappingSourceLast verified
No tentative-approval records are linked to this product.

Paragraph IV Challenges 0 records

Paragraph IV challenges below are sourced from legal records separately from FDA approvals. An ANDA filing, lawsuit or settlement does not establish final approval or commercial launch.

Application / productApplicantEvent / status Certification event date Product mappingSourceLast verified
No structured Paragraph IV certification events are linked in the available approval evidence.

Final ANDA Approvals 5 records

Approval dates do not establish commercial launch. Product mapping is shown for each linked record.

Application / productApplicantEvent / status Final approval date Product mappingSourceLast verified
216081 / 006JIANGSU HENGRUI PHARMACEUTICALS CO LTDFINAL_APPROVAL · FINAL_APPROVED2022-11-17 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217480 / 002HAINAN POLY PHARMACEUTICAL CO LTDFINAL_APPROVAL · FINAL_APPROVED2023-03-15 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219146 / 004ZENARA PHARMA PRIVATE LTDFINAL_APPROVAL · FINAL_APPROVED2026-06-08 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
219287 / 003VIWIT PHARMACEUTICAL CO LTDFINAL_APPROVAL · FINAL_APPROVED2026-06-11 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215957 / 004GE HEALTHCARE INCFINAL_APPROVAL · FINAL_APPROVED2026-06-29 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
PRODUCT_STATUS2011-03-14EXCLUSION_BASISMRI/MRA contrast agent; gadobutrol for CNS, breast, vascular and cardiac diagnostic imaging.Source
Independent legal-event information

Litigation & Settlement History

Settlement launch rights generally apply only to the named parties and product scope. These records do not change GenericRadar patent/exclusivity anchors or current decisions.

No litigation or settlement record currently linked to this product.