Application 018238

Type
NDA
Sponsor
NESHER PHARMS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001MICRO-KPOTASSIUM CHLORIDECAPSULE, EXTENDED RELEASE;ORAL8MEQYesNo
002MICRO-K 10POTASSIUM CHLORIDECAPSULE, EXTENDED RELEASE;ORAL10MEQYesNo

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N018238-001MICRO-KPOTASSIUM CHLORIDE8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982
N018238-002MICRO-K 10POTASSIUM CHLORIDE10MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 3 · 86 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 198284e616aacf4f…
2026-09-14 22:38:342026-08N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-1484e616aacf4f…
2026-08-18 06:07:402026-07N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982caaa826d4ba7…
2026-08-18 06:07:402026-07N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982011fe1cb6892…
2026-02-19 14:30 UTC2026-02N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 198231067a03dcf5…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-1431067a03dcf5…
2025-08-23 18:47 UTC2025-08N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19826a471c1ec25d…
2025-08-23 18:47 UTC2025-08N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-146a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982fd3edfee7708…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982b8a1b40f171c…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 198203ed91905a0d…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-1403ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19822680178bc6a6…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-142680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19825bbf6a4d5a75…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-145bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982d8e5a09893c0…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982d06236e962d9…
2024-10-29 15:01 UTC2024-10N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 198279d66fd596c7…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-1479d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 1982301d65b070ca…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-14301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19821e350fbaab3a…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-141e350fbaab3a…
2024-05-31 18:47 UTC2024-05N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19828072bd15b7f6…
2024-05-31 18:47 UTC2024-05N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-148072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N018238-001MICRO-K8MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19825c6f7cd8ea54…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06N018238-002MICRO-K 1010MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**CAPSULE, EXTENDED RELEASE / ORALRLD1984-05-145c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04N018238-001MICRO-K8MEQCAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19825d02ea3f76ae…
2022-04-08 23:34 UTC2022-04N018238-002MICRO-K 1010MEQCAPSULE, EXTENDED RELEASE / ORALRLD1984-05-145d02ea3f76ae…
2022-04-04 05:41 UTC2022-04N018238-001MICRO-K8MEQCAPSULE, EXTENDED RELEASE / ORALRLD, Approved before 19824b0b4de00fa7…
2022-04-04 05:41 UTC2022-04N018238-002MICRO-K 1010MEQCAPSULE, EXTENDED RELEASE / ORALRLD1984-05-144b0b4de00fa7…
2019-12-13 00:20 UTC2019-12N018238-001MICRO-K8MEQCAPSULE, EXTENDED RELEASE / ORALABRLD, Approved before 198274a2ff9319b5…
2019-12-13 00:20 UTC2019-12N018238-002MICRO-K 1010MEQCAPSULE, EXTENDED RELEASE / ORALABRLD1984-05-1474a2ff9319b5…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2019-12-13 00:20 UTC2019-12N018238-001AB174a2ff9319b5…
2019-12-13 00:20 UTC2019-12N018238-002AB174a2ff9319b5…
2019-12-14 00:12 UTC2019-12N018238-001AB13f01610625f2…
2019-12-14 00:12 UTC2019-12N018238-002AB13f01610625f2…
2019-09-15 20:21 UTC2019-09N018238-001AB1b00525d2431f…
2019-09-15 20:21 UTC2019-09N018238-002AB1b00525d2431f…
2019-07-19 19:46 UTC2019-07N018238-001AB1ea99ee380514…
2019-07-19 19:46 UTC2019-07N018238-002AB1ea99ee380514…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 10 · 196 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Potassium ChloridePOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC471f3a39-5fea-cd7a-e063-6294a90a0d932025-12-29Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDENorthwind Health Company, LLC0a72cc27-e092-d85a-e063-6294a90a503c2025-12-26Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDEBPI Labs LLCaeb2e14e-cd7c-49d0-a15f-fbbe89a03c6b2025-12-26Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
potassium chloridePOTASSIUM CHLORIDERedpharm Drug3735d41a-7787-6b92-e063-6294a90add452025-12-24Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
POKONZAPOTASSIUM CHLORIDECarwin Pharmaceutical Associates, LLC0700c19e-abca-4527-8944-e4440a32e3af2025-12-18Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDEIPG Pharmaceuticals, Inc.5dad0879-0f97-4c7d-98fa-baaed51cd2d82025-12-09Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDEGranules India Ltd113c031c-6de3-4497-a57d-9740b1ce08ac2025-12-02Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium Chloride for Oral SolutionPOTASSIUM CHLORIDEGranules Pharmaceuticals Inc.727be945-df2a-4fbf-ade4-f242e26479762025-12-02Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEGranules Pharmaceuticals Inc.302b3fa7-ea87-4bf1-aae0-6a2d7459de862025-12-02Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium chloridePOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC42773f05-7c2c-1790-e063-6294a90a78b32025-11-24Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEAurobindo Pharma Limitedb17d54ca-5885-48d3-96e9-b29ad14f8d762025-11-24Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium chloridePOTASSIUM CHLORIDEAdvagen Pharma Ltd8000e242-fe20-4d02-8f7d-97298857cf4c2025-11-19Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDEAvPAK6bb3f62d-79ce-cee6-8c6c-ee1eb6121f012025-11-19Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEAphena Pharma Solutions - Tennessee, LLC61fe55c2-fc9a-4fae-899a-06601baa78e12025-11-19Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEPD-Rx Pharmaceuticals, Inc.018fc687-1fba-202e-e063-6294a90a5c9a2025-11-17Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDEBluePoint Laboratories3709ee9a-f885-4a75-ab51-36e9e1ef04272025-11-10Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium ChloridePOTASSIUM CHLORIDEHenry Schein, Inc.8367a2ae-dfd9-4515-838c-529920291ca02025-11-07Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium Chloride Extended-ReleasePOTASSIUM CHLORIDEBryant Ranch Prepack2feda15e-f325-41fe-a442-41a8cc62b8552025-11-06Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium Chloride Extended-ReleasePOTASSIUM CHLORIDEA-S Medication Solutionsd486f982-a7d3-463d-a68d-89365ddaf5bb2025-11-06Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE
Potassium chloridePOTASSIUM CHLORIDEA-S Medication Solutions4a2173ba-556b-4ad7-be81-4da79b7394902025-11-06Warnings, Adverse reactionsName fallback
generic name: POTASSIUM CHLORIDE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

NDC Listings For This Application#

NDC listings for this application page 1 of 1 · 11 matching rows.

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0615-7646potassium chloridepotassium chlorideNCS HealthCare of KY, Inc dba Vangard LabsNDA AUTHORIZED GENERICCurrent
0615-7694potassium chloridepotassium chlorideNCS HealthCare of KY, Inc dba Vangard LabsNDA AUTHORIZED GENERICCurrent
51477-001potassium chloridepotassium chlorideNesher Pharmaceuticals (USA) LLCNDA AUTHORIZED GENERICCurrent
51477-002potassium chloridepotassium chlorideNesher Pharmaceuticals (USA) LLCNDA AUTHORIZED GENERICCurrent
68084-419potassium chloridepotassium chlorideAmerican Health PackagingNDA AUTHORIZED GENERICCurrent
68382-701POTASSIUM CHLORIDEpotassium chlorideZydus Pharmaceuticals (USA) Inc.NDA AUTHORIZED GENERICCurrent
68382-701POTASSIUM CHLORIDEpotassium chlorideZydus Pharmaceuticals (USA) Inc.NDA AUTHORIZED GENERICCurrent
68382-701POTASSIUM CHLORIDEpotassium chlorideZydus Pharmaceuticals (USA) Inc.NDA AUTHORIZED GENERICCurrent
68382-702POTASSIUM CHLORIDEpotassium chlorideZydus Pharmaceuticals (USA) Inc.NDA AUTHORIZED GENERICCurrent
68382-702POTASSIUM CHLORIDEpotassium chlorideZydus Pharmaceuticals (USA) Inc.NDA AUTHORIZED GENERICCurrent
68382-702POTASSIUM CHLORIDEpotassium chlorideZydus Pharmaceuticals (USA) Inc.NDA AUTHORIZED GENERICCurrent

Documents#

Document, Submission type, Date table
DocumentSubmission typeDate
53987SUPPL2018-05-03
53979SUPPL2018-05-02
40787SUPPL2009-01-12
40786SUPPL2009-01-12
14953SUPPL2003-08-25