NDC 80830-1691-01 - POTASSIUM PHOSPHATES

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
80830-1691
Requested NDC
80830-1691-01
Package NDCs from labels
80830-1691-3, 80830-1691-9, 80830-1691-6, 80830-1691-7, 80830-1691-1, 80830-1691-5, 80830-1691-2, 80830-1691-01
Manufacturer
Amneal Pharmaceuticals Private Limited
Effective date
2026-09-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
POTASSIUM PHOSPHATES - Amneal Pharmaceuticals Private LimitedAmneal Pharmaceuticals Private Limited2026-09-01HUMAN PRESCRIPTION DRUG LABEL
POTASSIUM PHOSPHATES - Amneal Pharmaceuticals Private LimitedAmneal Pharmaceuticals Private Limited2026-09-01HUMAN PRESCRIPTION DRUG LABEL
POTASSIUM PHOSPHATES - Amneal Pharmaceuticals Private LimitedAmneal Pharmaceuticals Private Limited2024-12-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80830-1691-1POTASSIUM PHOSPHATES15 mL in 1 VIAL, SINGLE-DOSESOLUTION, CONCENTRATE159
80830-1691-2POTASSIUM PHOSPHATES10 in 1 CARTONSOLUTION, CONCENTRATE109
80830-1691-5POTASSIUM PHOSPHATES25 in 1 CARTONSOLUTION, CONCENTRATE259
80830-1691-3POTASSIUM PHOSPHATES15 mL in 1 VIAL, SINGLE-DOSESOLUTION, CONCENTRATE151
80830-1691-6POTASSIUM PHOSPHATES15 mL in 1 VIAL, SINGLE-DOSESOLUTION, CONCENTRATE151
80830-1691-7POTASSIUM PHOSPHATES10 in 1 CARTONSOLUTION, CONCENTRATE101
80830-1691-9POTASSIUM PHOSPHATES10 in 1 CARTONSOLUTION, CONCENTRATE101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80830-1691POTASSIUM PHOSPHATES (POTASSIUM PHOSPHATE, MONOBASIC POTASSIUM PHOSPHATE, DIBASIC INJECTION,) SOLUTION, CONCENTRATE [AMNEAL PHARMACEUTICALS PRIVATE LIMITED]9Current NDC, 3 package rows20250108_89136c51-a60b-4269-bd05-9489f060a734.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80830-1691-1ML - Milliliter80830-1691eb311358-c9e8-45ba-b950-8bfe75b4fd8312023-12-05
80830-1691-2ML - Milliliter80830-16915a4c48ea-de13-4cdf-a26d-dbd82861809e12023-12-05

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 7 of 22 · 428 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ULINE EyewashEYEWASHNiagara Pharmaceuticals Inc.2d7f22d2-320b-6af1-e063-6294a90addc62025-11-24WarningsExact identifier
unii: 059QF0KO0R
Pur-WashEYEWASHNiagara Pharmaceuticals, Inc.0d43b1c1-2699-37f1-e054-00144ff88e882025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.777e1559-786f-8d54-e053-2991aa0aa98d2025-11-24WarningsExact identifier
unii: 059QF0KO0R
PUR-WASHWATERNiagara Pharmaceuticals Inc.7289103a-5cbf-42f4-8848-e827149a43ca2025-11-24WarningsExact identifier
unii: 059QF0KO0R
Helleborus comp. AHELLEBORUS COMP. AUriel Pharmacy Inc.150e57ad-3ed7-5cc9-e063-6394a90a25fe2025-11-21WarningsExact identifier
unii: 4J9FJ0HL51
Eyewash Additive ConcentrateWATER AND PROPYLENE GLYCOLHaws Corporationdd168403-398c-41ff-b1df-d93e4ff39de32025-11-20WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERFresenius Kabi USA, LLCfd823bef-c14c-4708-a18a-8aaa8470412f2025-11-18Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eyesaline Eyewash ConcentratePURIFIED WATERHoneywell Safety Products USA, Inc.3765c251-eb14-d60f-e063-6294a90a6a4d2025-11-12WarningsExact identifier
unii: 059QF0KO0R
Eyesaline Emergency EyewashPURIFIED WATERHoneywell Safety Products USA, Inc.37f244fd-c02f-e66a-e063-6394a90aed812025-11-12WarningsExact identifier
unii: 059QF0KO0R
STERILE WATERWATERHenry Schein, Inc.f4087143-9868-4308-b96c-43657ee8ec282025-11-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Bacteriostatic WaterBACTERIOSTATIC WATERProPharma Distribution42c6938e-f747-ae13-e063-6294a90a59a32025-11-04Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERICU Medical Inc.aab10f03-26ae-4dbc-a481-ef025e48b4052025-11-02Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERICU Medical Inc.e3484bc6-ed7f-43ef-9d49-c131a8dff2dd2025-11-02Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Ionosol MB and DextroseDEXTROSE MONOHYDRATE, SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM PHOSPHATE, MONOBASIC, AND SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATEICU Medical Inc.1b457b1d-0e80-4578-ba6f-dedf513fc9622025-10-30Warnings, Adverse reactionsExact identifier
unii: 4J9FJ0HL51
Sterile WaterWATERICU Medical Inc.1c0bbcb7-5ed6-4ee7-b297-080d3359474e2025-10-29Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Bacteriostatic WaterWATERHenry Schein, Inc.a833502e-a622-4e81-8c58-cef6ccb6c4c92025-10-27Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Miranda Castros Phosphorus 5 Cell Salts For Physical and Emotional Fatigue, Stress and TensionCALCAREA PHOS, FERRUM PHOS, KALI PHOS, MAGNESIUM PHOS, NATRUM PHOSMIRANDA CASTRO'S SHOP, LLC2670fdeb-0c80-9f23-e063-6394a90a8c6a2025-10-23WarningsExact identifier
unii: CI71S98N1Z
Sterile WaterWATERBecton Dickinson and Companycab03cda-4660-4020-a3be-bf86242ff6642025-10-22Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Potassium PhosphatesPOTASSIUM PHOSPHATESHospira, Inc.2fcbc814-c7a4-469a-8b1d-6819b961bfb92025-09-30Warnings, Adverse reactionsExact identifier
rxcui: 1928569
unii: CI71S98N1Z
unii: 4J9FJ0HL51
Xpect EyewashEYEWASHCintas Corporation1d69365d-662b-4248-8fa9-1629451b549a2025-09-30WarningsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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