NDC 0143-9935-91 - Cefotaxime

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: 0143-9935
Requested NDC: 0143-9935-91
Package NDCs from labels: 0143-9935-01, 0143-9935-91
Manufacturer: Hikma Pharmaceuticals USA Inc. | HIKMA FARMACEUTICA (PORTUGAL), S.A
Effective date: 2024-04-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cefotaxime - Hikma Pharmaceuticals USA Inc. \| HIKMA FARMACEUTICA (PORTUGAL), S.A	Hikma Pharmaceuticals USA Inc. \| HIKMA FARMACEUTICA (PORTUGAL), S.A	2024-04-11	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0143-9935-01	Cefotaxime	1 in 1 PACKAGE	INJECTION	1		9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0143-9935	CEFOTAXIME INJECTION [HIKMA PHARMACEUTICALS USA INC.]	9	Current NDC, Legacy NDC, 1 package rows	20240413_ef1a6dc6-bc3d-4f09-8f92-7ff328f56561.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0143-9935-01	EA - Each	0143-9935	e75c7c19-3c60-4f5d-b183-0848875b43bb	1	2015-12-02
0143-9935-91	EA - Each	0143-9935	e8dfeca5-2e69-4eba-9faa-ce3bd9d5250b	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
CEFOTAXIME SODIUM	ACTIVE INGREDIENT	258J72S7TZ	CEFOTAXIME INJECTION [WEST-WARD PHARMACEUTICAL CORP]	7
CEFOTAXIME	ACTIVE MOIETY	N2GI8B1GK7	CEFOTAXIME INJECTION [WEST-WARD PHARMACEUTICAL CORP]	7

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 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cefotaxime	CEFOTAXIME INJECTION	SteriMax Inc.	8efe3bd0-c43a-2bd6-e053-2a95a90a92fa	2026-06-15		Exact identifier unii: 258J72S7TZ
Cefotaxime	CEFOTAXIME	Hikma Pharmaceuticals USA Inc.	ed23b6bc-32c7-4c50-a53d-313ae78e5623	2024-04-11	Warnings, Adverse reactions	Exact identifier unii: 258J72S7TZ
Cefotaxime	CEFOTAXIME	Hikma Pharmaceuticals USA Inc.	ef1a6dc6-bc3d-4f09-8f92-7ff328f56561	2024-04-11	Warnings, Adverse reactions	Exact identifier application number: ANDA065071 ndc (package): 0143-9935-01 ndc (product): 0143-9935 rxcui: 309065 spl id: e25af43f-54cb-4526-a8a5-6bef0a7939c7 spl set id: ef1a6dc6-bc3d-4f09-8f92-7ff328f56561 unii: 258J72S7TZ

Reported adverse events (FAERS/openFDA)#

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