NDC 71285-0003-1

This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.

Requested NDC
71285-0003-1
Product root
71285-0003
Identity scope
Package
Primary current NDC product row
Not present

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
compounderpackage71285-000371285-0003-1COMPOUNDEROutsourcing facility compounded drug report2020-12026-10-13
compounderpackage71285-000371285-0003-1COMPOUNDEROutsourcing facility compounded drug report2019-22026-10-13
compounderpackage71285-000371285-0003-1COMPOUNDEROutsourcing facility compounded drug report2019-12026-10-13

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 3 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-08-27 00:00 UTC · source 2025-08-20compounderpackage71285-000371285-0003-1COMPOUNDEROutsourcing facility compounded drug report2020-1compounder / compounders_ndc_directory.zipaf8e9b524e63…ca326a94a5e9…
2025-08-27 00:00 UTC · source 2025-08-20compounderpackage71285-000371285-0003-1COMPOUNDEROutsourcing facility compounded drug report2019-2compounder / compounders_ndc_directory.zipaf8e9b524e63…ca326a94a5e9…
2025-08-27 00:00 UTC · source 2025-08-20compounderpackage71285-000371285-0003-1COMPOUNDEROutsourcing facility compounded drug report2019-1compounder / compounders_ndc_directory.zipaf8e9b524e63…ca326a94a5e9…

Compounder NDC reports#

Browse the complete compounder directory for this NDC · Browse every current compounder row in the unified auxiliary catalog · browse compounder source captures and parsed snapshots.

Establishment, FEI, Product NDC table
EstablishmentFEIProduct NDCPackage NDCProductActive ingredientsReporting periodNormalization
"Central Admixture Pharmacy Services, Inc.(019684530)"71285-000371285-0003-1"dextrose Monohydrate; Potassium Chloride; Aspartic Acid; Trisodium Citrate Dihydrate; Sodium Phosphate, Monobasic, Monohydrate; Anhydrous Dextrose; Citric Acid Monohydrate; Tromethamine; Glutamic Acid"25.27 g/1000 mL; 80 meq/1000 mL; 9.8 g/1000 mL; 59.175 g/1000 mL; 4.995 g/1000 mL; 104.4 g/1000 mL; 7.3575 g/1000 mL; 8.1 g/1000 mL; 10.7 g/1000 mL2020-1valid
"Central Admixture Pharmacy Services, Inc.(019684530)"71285-000371285-0003-1"dextrose Monohydrate; Potassium Chloride; Aspartic Acid; Trisodium Citrate Dihydrate; Sodium Phosphate, Monobasic, Monohydrate; Anhydrous Dextrose; Citric Acid Monohydrate; Tromethamine; Glutamic Acid"25.27 g/1000 mL; 80 meq/1000 mL; 9.8 g/1000 mL; 59.175 g/1000 mL; 4.995 g/1000 mL; 104.4 g/1000 mL; 7.3575 g/1000 mL; 8.1 g/1000 mL; 10.7 g/1000 mL2019-2valid
"Central Admixture Pharmacy Services, Inc.(019684530)"71285-000371285-0003-1"dextrose Monohydrate; Potassium Chloride; Aspartic Acid; Trisodium Citrate Dihydrate; Sodium Phosphate, Monobasic, Monohydrate; Anhydrous Dextrose; Citric Acid Monohydrate; Tromethamine; Glutamic Acid"25.27 g/1000 mL; 80 meq/1000 mL; 9.8 g/1000 mL; 59.175 g/1000 mL; 4.995 g/1000 mL; 104.4 g/1000 mL; 7.3575 g/1000 mL; 8.1 g/1000 mL; 10.7 g/1000 mL2019-1valid

Reported adverse events (FAERS/openFDA)#

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