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Product profile · United States

PHENYLEPHRINE HYDROCHLORIDE

 ·  Patent Litigation & Settlement History ↓

IngredientPHENYLEPHRINE HYDROCHLORIDE
Application typeNDA
Application203826
Product002
Dosage formSOLUTION
RouteINTRAVENOUS
Strength50MG/5ML (10MG/ML)
Approval date2019-06-19
Marketing statusPrescription
Status event—
ApplicantHIKMA PHARMS
Product source

Current GenericRadar decision

Year2023
SelectionEXISTING_GENERIC
ReviewDISQUALIFIED
Anchor typeFINAL_ANDA
Anchor date2023-06-26
Patent anchor—
Exclusivity anchor—
Protection date—
First Final ANDA2023-06-26
Status event—

Exact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.

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
210333 / 001FINAL_APPROVAL · FINAL_APPROVED2018-04-27—MEITHEAL PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211078 / 001FINAL_APPROVAL · FINAL_APPROVED2018-07-19—AMNEAL EU LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210025 / 002FINAL_APPROVAL · FINAL_APPROVED2018-12-21—PH HEALTH LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210666 / 001FINAL_APPROVAL · FINAL_APPROVED2019-01-30—FRESENIUS KABI USA LLCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
208905 / 002FINAL_APPROVAL · FINAL_APPROVED2019-01-31—SANDOZ INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
209967 / 002FINAL_APPROVAL · FINAL_APPROVED2020-01-16—SAGENT PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211920 / 001FINAL_APPROVAL · FINAL_APPROVED2020-06-05—GLAND PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213318 / 002FINAL_APPROVAL · FINAL_APPROVED2020-06-11—CAPLIN STERILES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
213237 / 002FINAL_APPROVAL · FINAL_APPROVED2020-07-01—ACCORD HEALTHCARE INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
211081 / 002FINAL_APPROVAL · FINAL_APPROVED2020-07-17—MILLA PHARMACEUTICALS INCNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
210697 / 001FINAL_APPROVAL · FINAL_APPROVED2020-11-13—EUGIA PHARMA SPECIALITIES LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217069 / 002FINAL_APPROVAL · FINAL_APPROVED2022-08-30—MANKIND PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217521 / 002FINAL_APPROVAL · FINAL_APPROVED2023-06-26—BE PHARMACEUTICALS AGNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218412 / 002FINAL_APPROVAL · FINAL_APPROVED2024-03-14—HAINAN POLY PHARM CO LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
218110 / 002FINAL_APPROVAL · FINAL_APPROVED2024-05-10—ASPIRO PHARMA LTDNEXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource
217032 / 002FINAL_APPROVAL · FINAL_APPROVED2026-04-03—BAXTER HEALTHCARE CORPNEXACT_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 16 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
210333 / 001MEITHEAL PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2018-04-27 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211078 / 001AMNEAL EU LTDFINAL_APPROVAL · FINAL_APPROVED2018-07-19 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210025 / 002PH HEALTH LTDFINAL_APPROVAL · FINAL_APPROVED2018-12-21 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210666 / 001FRESENIUS KABI USA LLCFINAL_APPROVAL · FINAL_APPROVED2019-01-30 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
208905 / 002SANDOZ INCFINAL_APPROVAL · FINAL_APPROVED2019-01-31 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
209967 / 002SAGENT PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2020-01-16 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211920 / 001GLAND PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2020-06-05 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213318 / 002CAPLIN STERILES LTDFINAL_APPROVAL · FINAL_APPROVED2020-06-11 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
213237 / 002ACCORD HEALTHCARE INCFINAL_APPROVAL · FINAL_APPROVED2020-07-01 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
211081 / 002MILLA PHARMACEUTICALS INCFINAL_APPROVAL · FINAL_APPROVED2020-07-17 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
210697 / 001EUGIA PHARMA SPECIALITIES LTDFINAL_APPROVAL · FINAL_APPROVED2020-11-13 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217069 / 002MANKIND PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2022-08-30 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217521 / 002BE PHARMACEUTICALS AGFINAL_APPROVAL · FINAL_APPROVED2023-06-26 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218412 / 002HAINAN POLY PHARM CO LTDFINAL_APPROVAL · FINAL_APPROVED2024-03-14 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
218110 / 002ASPIRO PHARMA LTDFINAL_APPROVAL · FINAL_APPROVED2024-05-10 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
217032 / 002BAXTER HEALTHCARE CORPFINAL_APPROVAL · FINAL_APPROVED2026-04-03 EXACT_PRODUCT · PENDING_PRODUCT_MAPPINGSource—
Decision evidence (1)
TypeDateRoleBasisSource
GENERIC2023-06-26TERMINAL_GENERIC_BASISExact product/strength Final ANDA confirmed. Date is earliest verified official product approval for the batch. AG and tentative excluded. Approval date is not commercial launch date. No DS classification asserted.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.