ANTICOAGULANT SODIUM CITRATE

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: ANTICOAGULANT SODIUM CITRATE
Generic name: TRISODIUM CITRATE DIHYDRATE
Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
SPL set ID: 7025a0f9-1a56-4416-a3a4-925d755aed90
SPL ID: 8855e600-2002-4c8b-94dc-d275de33169b
Version: 4
Effective date: 2024-04-02
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:17:22

Harmonized routes table
Harmonized routes
EXTRACORPOREAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		BN980123	openfda.application_number
brand name		ANTICOAGULANT SODIUM CITRATE	openfda.brand_name
generic name		TRISODIUM CITRATE DIHYDRATE	openfda.generic_name
manufacturer name		Baxter Healthcare Corporation	openfda.manufacturer_name
ndc	package	0338-9669-01	openfda.package_ndc
ndc	product	0338-9669	openfda.product_ndc
ndc11	package	00338966901	derived:openfda.package_ndc
spl id		8855e600-2002-4c8b-94dc-d275de33169b	id
spl set id		7025a0f9-1a56-4416-a3a4-925d755aed90	set_id
unii		B22547B95K	openfda.unii

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