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Product profile · United States

CARDENE IV IN DEXTROSE

 ·  Patent Litigation & Settlement History ↓

Ingredient—
Application typeNDA
Application019734
Product005
Dosage form—
Route—
Strength40MG/200ML
Approval date2008-11-07
Marketing status—
Status event—
Applicant—
Product source

Current GenericRadar decision

Year2008
SelectionDEEP_REVIEW
ReviewDEEP_REVIEW
Anchor type—
Anchor date—
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA—
Status event—

CARDENE IV in Dextrose NDA 019734: no adopted TRUE_DS or DS-equivalent patent, no identified whole-product exclusivity anchor. Product approval is in 2008; later DP/U patent tail warrants DEEP_REVIEW. 2027-12-26 DP expiry is not a DS anchor. User-directed judgment 2026-10-23.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
76592912027-04-18U U-1029NNU
FDA listing only: DP/U not promoted to TRUE_DS or DS-equivalent. Existing judgment unchanged.
———
84555242027-04-18U U-1029NNU
FDA listing only: DP/U not promoted to TRUE_DS or DS-equivalent. Existing judgment unchanged.
———
76121022027-12-26DP —NNDP
FDA listing only: DP/U not promoted to TRUE_DS or DS-equivalent. Existing judgment unchanged.
———
93645642027-12-26DP —NNDP
FDA listing only: DP/U not promoted to TRUE_DS or DS-equivalent. Existing judgment unchanged.
———

Regulatory exclusivity

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
No generic approval facts are linked to this product.

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 0 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
No final-approval records are linked to this product.
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.