REGIOCIT
REGIOCIT
Approved
Approval ID
6fa432f1-7cde-4840-80f0-1be19a76f318
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 13, 2020
Manufacturers
FDA
Baxter Healthcare Corporation
DUNS: 005083209
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Sodium Chloride, Sodium Citrate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code24571-123
Product Classification
G
Generic Name
Sodium Chloride, Sodium Citrate
Product Specifications
Route of AdministrationEXTRACORPOREAL
Effective DateAugust 13, 2020
FDA Product Classification
INGREDIENTS (4)
SODIUM CHLORIDEActive
Quantity: 5.03 g in 1000 mL
Code: 451W47IQ8X
Classification: ACTIB
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CITRATE, UNSPECIFIED FORMActive
Quantity: 5.29 g in 1000 mL
Code: 1Q73Q2JULR
Classification: ACTIB