NDC 68084-850-33 - Potassium Citrate

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
68084-850
Requested NDC
68084-850-33
Package NDCs from labels
68084-850-33, 68084-850-32
Manufacturer
American Health Packaging
Effective date
2024-09-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Potassium Citrate - American Health PackagingAmerican Health Packaging2024-09-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68084-850-32Potassium Citrate20 in 1 BOX, UNIT-DOSETABLET, EXTENDED RELEASE206
68084-850-33Potassium Citrate1 in 1 BLISTER PACKTABLET, EXTENDED RELEASE16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68084-850POTASSIUM CITRATE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING]6Current NDC, Legacy NDC, 2 package rows20240905_1201c777-2388-4235-bb8f-eb7dc1e867f8.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68084-850-32EA - Each68084-8502d5ade25-88ae-4904-961a-35ed3819ae1c12014-11-05
68084-850-33EA - Each68084-850eed1def1-0d4f-4297-91da-f495abad7c9d12014-11-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
POTASSIUM CITRATEACTIVE INGREDIENTEE90ONI6FFPOTASSIUM CITRATE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING]2
ANHYDROUS CITRIC ACIDACTIVE MOIETYXF417D3PSLPOTASSIUM CITRATE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING]2
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZPOTASSIUM CITRATE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING]2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30POTASSIUM CITRATE TABLET, EXTENDED RELEASE [AMERICAN HEALTH PACKAGING]2

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 1 of 2 · 38 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
POTASSIUM CITRATEPOTASSIUM CITRATERising Pharma Holdings, Inc.164d9d05-fbb1-4d99-8ba3-ff9c172aa8ca2026-07-14Warnings, Adverse reactionsExact identifier
rxcui: 199381
rxcui: 199376
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEBryant Ranch Prepackff67f638-5b53-406a-962a-87773a91fc482026-05-26Warnings, Adverse reactionsExact identifier
rxcui: 199381
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEREMEDYREPACK INC.a9cc636d-3e26-450c-9df8-665d530d626f2026-04-06Warnings, Adverse reactionsExact identifier
rxcui: 199381
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEBryant Ranch Prepack6271d84e-d991-4bb8-ac9f-6d5cc879b6312026-03-25Warnings, Adverse reactionsExact identifier
rxcui: 898490
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEBryant Ranch Prepack595343aa-b760-4158-9c49-dd5368f45e2c2026-03-25Warnings, Adverse reactionsExact identifier
rxcui: 199381
unii: EE90ONI6FF
TricitratesTRICITRATESChartwell Governmental & Specialty RX, LLC.c4ff0407-3930-4c48-afd4-d2cb3e1b18f42026-02-25Warnings, Adverse reactionsExact identifier
unii: EE90ONI6FF
Potassium Citrate and Citric AcidPOTASSIUM CITRATE AND CITRIC ACIDChartwell Governmental & Specialty RX, LLC.fd57a176-7faf-4053-b348-6ba5f192f05a2026-02-25Warnings, Adverse reactionsExact identifier
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEANI Pharmaceuticals, Inc.2fb31727-68b1-4183-947d-00e08bf999872025-12-22Warnings, Adverse reactionsExact identifier
rxcui: 199381
rxcui: 898490
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEBiocomp Pharma, Inc.b32fe71a-4a58-04a1-64d3-bc3cc4a895bf2025-12-16Warnings, Adverse reactionsExact identifier
rxcui: 199381
rxcui: 898490
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEBryant Ranch Prepackebf1f1f1-4458-4d34-8432-21698a550e072025-11-04Warnings, Adverse reactionsExact identifier
rxcui: 199381
unii: EE90ONI6FF
POTASSIUM CITRATE EXTENDED RELEASEPOTASSIUM CITRATEBryant Ranch Prepack3dd9c9eb-df19-4ec9-bc77-f3a159b33d942025-10-23Warnings, Adverse reactionsExact identifier
rxcui: 199381
unii: EE90ONI6FF
POTASSIUM CITRATEPOTASSIUM CITRATEBryant Ranch Prepackb3ccba22-48cd-45f8-8c72-b80f34fe56be2025-10-23Warnings, Adverse reactionsExact identifier
rxcui: 898490
unii: EE90ONI6FF
POTASSIUM CITRATE EXTENDED RELEASEPOTASSIUM CITRATEBryant Ranch Prepack44ab2c4f-4a76-470d-98fb-8874c692a9672025-08-20Warnings, Adverse reactionsExact identifier
rxcui: 199376
unii: EE90ONI6FF
Potassium CitratePOTASSIUM CITRATEUpsher-Smith Laboratories, LLC2215dc1d-0b5a-469e-9b51-4d7480a510782025-07-14Warnings, Adverse reactionsExact identifier
rxcui: 199381
rxcui: 199376
unii: EE90ONI6FF
POTASSIUM CITRATE EXTENDED RELEASEPOTASSIUM CITRATEStrides Pharma Inc.5f38b02c-703c-4fc2-b833-654e41bd617f2025-07-01Warnings, Adverse reactionsExact identifier
rxcui: 199381
rxcui: 898490
rxcui: 199376
unii: EE90ONI6FF
POTASSIUM CITRATE EXTENDED RELEASEPOTASSIUM CITRATEBryant Ranch Prepack8f5f7078-3c2d-406f-9222-b82a0f79d1682025-05-02Warnings, Adverse reactionsExact identifier
rxcui: 898490
unii: EE90ONI6FF
POTASSIUM CITRATE EXTENDED RELEASEPOTASSIUM CITRATEBryant Ranch Prepackb6ce81aa-ed9e-4eac-9f9c-26e2560f06db2025-05-02Warnings, Adverse reactionsExact identifier
rxcui: 199381
unii: EE90ONI6FF
TricitratesTRICITRATESChartwell RX, LLC2a80ea6b-6334-4c33-a35e-a5cb2939fbcb2025-04-28Warnings, Adverse reactionsExact identifier
unii: EE90ONI6FF
Potassium Citrate and Citric AcidPOTASSIUM CITRATE AND CITRIC ACIDChartwell RX, LLC978a5a9d-f0ca-4308-a84b-3b132263bbb82025-04-09Warnings, Adverse reactionsExact identifier
unii: EE90ONI6FF
POTASSIUM CITRATEPOTASSIUM CITRATEBryant Ranch Prepack012c925e-5874-472b-a675-00bf79f649802024-12-24Warnings, Adverse reactionsExact identifier
rxcui: 898490
unii: EE90ONI6FF

Reported adverse events (FAERS/openFDA)#

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