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Product profile · United States

DAPTOMYCIN

 ·  Patent Litigation & Settlement History ↓

IngredientDAPTOMYCIN
Application typeNDA
Application210282
Product002
Dosage formPOWDER
RouteINTRAVENOUS
Strength500MG/VIAL
Approval date2021-06-21
Marketing statusPrescription
Status event—
ApplicantHOSPIRA
Product source

Current GenericRadar decision

Year2033
SelectionCANDIDATE
ReviewFINAL
Anchor typeDS_EQUIVALENT_PATENT
Anchor date2033-09-11
Patent anchor2033-09-11
Exclusivity anchor—
Protection date2033-09-11
First Final ANDA—
Status event—

US9655946 claim 18 and US10357535 claim 12 cover bacterial-infection treatment, compared against the NDA210282 citric-acid label. Internal DS-equivalent interpretation. No later tail identified. Citric-acid concentrations for 350 mg/7 mL and 500 mg/10 mL are approximately 40 mM, within the claim 1 range of 10-500 mM. Broad bacterial-infection use claims are considered difficult to avoid solely by indication carve-out. Formulation changes require separate FTO assessment. 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
103575352033-09-11DP/U U-3176NYDS_EQUIVALENT
[GNR_US204_50] Claim 12: bacterial-infection treatment; claim 1: 200-600 mg plus citric acid and reconstitution in 5-15 mL. Internal full-label use-claim interpretation.
———
103575352033-09-11DP/U U-3176NYDS_EQUIVALENT
Claim 12: bacterial-infection treatment; claim 1: 200-600 mg plus citric acid and reconstitution in 5-15 mL. Internal full-label use-claim interpretation.
———
96559462033-09-11DP/U U-3175NYDS_EQUIVALENT
[GNR_US204_50] Claim 18: bacterial-infection treatment plus product citric-acid formulation. Internal full-label use-claim interpretation.
———
96559462033-09-11DP/U U-3175NYDS_EQUIVALENT
Claim 18: bacterial-infection treatment plus product citric-acid formulation. Internal full-label use-claim interpretation.
———

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
202857 / 001FINAL_APPROVAL · FINAL_APPROVED2014-09-12—HOSPIRA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
091039 / 001FINAL_APPROVAL · FINAL_APPROVED2016-03-25—TEVA PHARMACEUTICALS USA INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
206005 / 001FINAL_APPROVAL · FINAL_APPROVED2016-06-15—XELLIA PHARMACEUTICALS APSNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
206077 / 001FINAL_APPROVAL · FINAL_APPROVED2018-04-11—FRESENIUS KABI USA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
205037 / 001FINAL_APPROVAL · FINAL_APPROVED2018-06-05—MYLAN LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
208375 / 001FINAL_APPROVAL · FINAL_APPROVED2019-05-01—DR REDDYS LABORATORIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211961 / 001FINAL_APPROVAL · FINAL_APPROVED2019-06-24—ACCORD HEALTHCARE INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
212513 / 001FINAL_APPROVAL · FINAL_APPROVED2019-06-26—BE PHARMACEUTICALS AGNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
212022 / 001FINAL_APPROVAL · FINAL_APPROVED2019-08-22—JIANGSU HENGRUI PHARMACEUTICALS CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
207104 / 001FINAL_APPROVAL · FINAL_APPROVED2019-11-15—SAGENT PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
212250 / 001FINAL_APPROVAL · FINAL_APPROVED2021-04-21—HISUN PHARMACEUTICAL HANGZHOU CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213623 / 001FINAL_APPROVAL · FINAL_APPROVED2021-06-29—MEITHEAL PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215316 / 001FINAL_APPROVAL · FINAL_APPROVED2021-08-24—QILU PHARMACEUTICAL HAINAN CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213171 / 001FINAL_APPROVAL · FINAL_APPROVED2021-09-02—EUGIA PHARMA SPECIALITIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215215 / 001FINAL_APPROVAL · FINAL_APPROVED2021-11-26—HANGZHOU ZHONGMEI HUADONG PHARMACEUTICAL CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
215890 / 001FINAL_APPROVAL · FINAL_APPROVED2022-08-18—HAINAN POLY PHARMACEUTICAL CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
216413 / 001FINAL_APPROVAL · FINAL_APPROVED2022-09-23—ASPIRO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213966 / 001FINAL_APPROVAL · FINAL_APPROVED2023-08-07—MYLAN PHARMACEUTICALS INC A VIATRIS CONEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217215 / 001FINAL_APPROVAL · FINAL_APPROVED2024-08-29—BIOCON PHARMA LTDNEXACT_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 19 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
202857 / 001HOSPIRA INCFINAL_APPROVAL · FINAL_APPROVED2014-09-12 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
091039 / 001TEVA PHARMACEUTICALS USA INCFINAL_APPROVAL · FINAL_APPROVED2016-03-25 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
206005 / 001XELLIA PHARMACEUTICALS APSFINAL_APPROVAL · FINAL_APPROVED2016-06-15 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
206077 / 001FRESENIUS KABI USA LLCFINAL_APPROVAL · FINAL_APPROVED2018-04-11 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
205037 / 001MYLAN LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2018-06-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
208375 / 001DR REDDYS LABORATORIES LTDFINAL_APPROVAL · FINAL_APPROVED2019-05-01 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211961 / 001ACCORD HEALTHCARE INCFINAL_APPROVAL · FINAL_APPROVED2019-06-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
212513 / 001BE PHARMACEUTICALS AGFINAL_APPROVAL · FINAL_APPROVED2019-06-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
212022 / 001JIANGSU HENGRUI PHARMACEUTICALS CO LTDFINAL_APPROVAL · FINAL_APPROVED2019-08-22 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
207104 / 001SAGENT PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2019-11-15 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
212250 / 001HISUN PHARMACEUTICAL HANGZHOU CO LTDFINAL_APPROVAL · FINAL_APPROVED2021-04-21 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213623 / 001MEITHEAL PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2021-06-29 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215316 / 001QILU PHARMACEUTICAL HAINAN CO LTDFINAL_APPROVAL · FINAL_APPROVED2021-08-24 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213171 / 001EUGIA PHARMA SPECIALITIES LTDFINAL_APPROVAL · FINAL_APPROVED2021-09-02 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215215 / 001HANGZHOU ZHONGMEI HUADONG PHARMACEUTICAL CO LTDFINAL_APPROVAL · FINAL_APPROVED2021-11-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
215890 / 001HAINAN POLY PHARMACEUTICAL CO LTDFINAL_APPROVAL · FINAL_APPROVED2022-08-18 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
216413 / 001ASPIRO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2022-09-23 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213966 / 001MYLAN PHARMACEUTICALS INC A VIATRIS COFINAL_APPROVAL · FINAL_APPROVED2023-08-07 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217215 / 001BIOCON PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2024-08-29 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (2)
TypeDateRoleBasisSource
PATENT2033-09-11LISTING_CONTEXTClaim 18: bacterial-infection treatment plus product citric-acid formulation. Internal full-label use-claim interpretation.Source
PATENT2033-09-11CANONICAL_ANCHORClaim 12: bacterial-infection treatment; claim 1: 200-600 mg plus citric acid and reconstitution in 5-15 mL. Internal full-label use-claim interpretation.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.