NDC 70594-112-01 - Carboprost Tromethamine

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: 70594-112
Requested NDC: 70594-112-01
Package NDCs from labels: 70594-112-01, 70594-112-02
Manufacturer: Xellia Pharmaceuticals USA LLC | Steriscience Pte. Limited | Stelis Biopharma Limited
Effective date: 2023-11-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Carboprost Tromethamine Injection, USP	Xellia Pharmaceuticals USA LLC \| Steriscience Pte. Limited \| Stelis Biopharma Limited	2023-11-01	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70594-112-01	Carboprost Tromethamine	1 mL in 1 VIAL	SOLUTION	1		2
70594-112-02	Carboprost Tromethamine	10 in 1 CARTON	SOLUTION	10		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70594-112	CARBOPROST TROMETHAMINE SOLUTION [XELLIA PHARMACEUTICALS USA LLC]	2	Current NDC, 2 package rows	20231108_8a1284cf-002f-4887-a3c0-d73d04b2b869.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70594-112-01	ML - Milliliter	70594-112	8a616d81-cdb1-461d-909f-5a70ea3f6fad	1	2024-02-14
70594-112-02	ML - Milliliter	70594-112	d16e2a4c-f4d3-4011-9101-8afdfdd2e959	1	2024-02-14

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 2 of 2 · 23 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CARBOPROST TROMETHAMINE	CARBOPROST TROMETHAMINE	BE Pharmaceuticals Inc.	8447d4f1-d286-4aa0-a379-a673518da045	2023-05-09	Adverse reactions	Exact identifier rxcui: 238014 unii: U4526F86FJ
CARBOPROST TROMETHAMINE	CARBOPROST TROMETHAMINE	Fresenius Kabi USA, LLC	e5f58209-bc3d-4d9f-a372-bc14f877d16c	2023-05-05	Adverse reactions	Exact identifier rxcui: 238014 unii: U4526F86FJ
Carboprost Tromethamine	CARBOPROST TROMETHAMINE	Long Grove Pharmaceuticals, LLC	f0b2d3f9-859a-47bb-866c-082717d1f190	2022-10-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 238014 unii: U4526F86FJ

Reported adverse events (FAERS/openFDA)#

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