FDA Product

REGIOCIT

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Product Name

REGIOCIT

FDA Product Code

24571-123

Regulatory Information

NDC Product Code

24571-123

Effective Date

August 13, 2020

FDA Title

REGIOCIT

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Version Number

4

Company Information

ManufacturerBaxter Healthcare Corporation

DUNS Number

005083209

Active Ingredients

SODIUM CHLORIDE

Quantity: 5.03 g in 1000 mL

Code: 451W47IQ8X

Class Code: ACTIB

HYDROCHLORIC ACID

Code: QTT17582CB

Class Code: IACT

WATER

Code: 059QF0KO0R

Class Code: IACT

SODIUM CITRATE, UNSPECIFIED FORM

Quantity: 5.29 g in 1000 mL

Code: 1Q73Q2JULR

Class Code: ACTIB

Active Moieties

SODIUM CATION

Code: LYR4M0NH37

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