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Product profile · United States

DAPTOMYCIN

 ·  Patent Litigation & Settlement History ↓

IngredientDAPTOMYCIN
Application typeNDA
Application217415
Product001
Dosage formPOWDER
RouteINTRAVENOUS
Strength350MG/VIAL
Approval date2023-01-30
Marketing statusPrescription
Status event—
ApplicantHIKMA PHARMS
Product source

Current GenericRadar decision

Year2038
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeDS_EQUIVALENT_PATENT
Anchor date2038-08-28
Patent anchor2038-08-28
Exclusivity anchor—
Protection date2043-01-09
First Final ANDA—
Status event—

US12053502 claims 1/2 cover Gram-positive infections, compared against the NDA217415 histidine/arginine label. Internal DS-equivalent interpretation. US12629337 DP tail expires 2043-01-09, after the anchor. Human-treatment claims have no age restriction and include pediatric scope. Label molecular weights/excipients imply a DAP:His:Arg molar ratio of approximately 1:3:5. Measured stability and design-around feasibility remain evidence limitations. Evidence limits: complete comparison of unverified ANDA candidates against original RLD documents remains incomplete; absence of generics is not established; complete historical patent/exclusivity collection remains incomplete; all-indication use claims are interpreted as DS-equivalent in the decision; formulation design-around feasibility and claim stability requirements require further assessment.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
117594972038-08-28DP —NNDP
[GNR_US204_50] Claim 1: histidine plus amino-acid composition and stability limitations.
———
117594972038-08-28DP —NNDP
Claim 1: histidine plus amino-acid composition and stability limitations.
———
120535022038-08-28U U-3981NYDS_EQUIVALENT
[GNR_US204_50] Claim 1: Gram-positive infection treatment; claim 2: cSSSI and S. aureus bloodstream infections; no human age restriction. Product measurements for stability conditions are unavailable.
———
120535022038-08-28U U-3981NYDS_EQUIVALENT
Claim 1: Gram-positive infection treatment; claim 2: cSSSI and S. aureus bloodstream infections; no human age restriction. Product measurements for stability conditions are unavailable.
———
126293372043-01-09DP —NNDP
[GNR_US204_50] Claim 1: branched-chain amino-acid formulation and reconstitution-time limitations.
———
126293372043-01-09DP —NNDP
Claim 1: branched-chain amino-acid formulation and reconstitution-time limitations.
———

Regulatory exclusivity

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

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

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

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
212667 / 001FINAL_APPROVAL · FINAL_APPROVED2019-07-12—ACCORD HEALTHCARE INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213425 / 001FINAL_APPROVAL · FINAL_APPROVED2020-08-20—BE PHARMACEUTICALS AGNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211403 / 001FINAL_APPROVAL · FINAL_APPROVED2020-08-31—DR REDDYS LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213786 / 001FINAL_APPROVAL · FINAL_APPROVED2021-06-29—MEITHEAL PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
216445 / 001FINAL_APPROVAL · FINAL_APPROVED2022-12-23—ASPIRO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213396 / 001FINAL_APPROVAL · FINAL_APPROVED2024-08-01—FRESENIUS KABI USA LLCNEXACT_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 6 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
212667 / 001ACCORD HEALTHCARE INCFINAL_APPROVAL · FINAL_APPROVED2019-07-12 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213425 / 001BE PHARMACEUTICALS AGFINAL_APPROVAL · FINAL_APPROVED2020-08-20 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211403 / 001DR REDDYS LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2020-08-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213786 / 001MEITHEAL PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2021-06-29 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
216445 / 001ASPIRO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2022-12-23 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213396 / 001FRESENIUS KABI USA LLCFINAL_APPROVAL · FINAL_APPROVED2024-08-01 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (3)
TypeDateRoleBasisSource
PATENT2038-08-28CANONICAL_ANCHORClaim 1: Gram-positive infection treatment; claim 2: cSSSI and S. aureus bloodstream infections; no human age restriction. Product measurements for stability conditions are unavailable.Source
PATENT2038-08-28LISTING_CONTEXTClaim 1: histidine plus amino-acid composition and stability limitations.Source
PATENT2043-01-09FTO_TAILClaim 1: branched-chain amino-acid formulation and reconstitution-time limitations.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.