NDC 0781-9404-85 - Ampicillin

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: 0781-9404
Requested NDC: 0781-9404-85
Package NDCs from labels: 0781-9404-85, 0781-9404-95
Manufacturer: Sandoz Inc
Effective date: 2024-10-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ampicillin - Sandoz Inc	Sandoz Inc	2024-10-31	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
0781-9404-85	Ampicillin	1 in 1 VIAL, GLASS	INJECTION, POWDER, FOR SOLUTION	1		23
0781-9404-95	Ampicillin	10 in 1 PACKAGE	INJECTION, POWDER, FOR SOLUTION	10		23

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0781-9404	AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]	23	Current NDC, Legacy NDC, 2 package rows	20250426_b371e1a5-1fef-4df2-8940-c4fc02b9e2f0.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0781-9404-85	EA - Each	0781-9404	4362c369-18df-499d-b17f-e75704ade872	1	2012-07-24
0781-9404-95	EA - Each	0781-9404	e6eedebd-e102-470c-90ef-c64ef4daa61c	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
AMPICILLIN SODIUM	ACTIVE INGREDIENT	JFN36L5S8K	AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]	14
AMPICILLIN	ACTIVE MOIETY	7C782967RD	AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SANDOZ INC]	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 4 of 4 · 62 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ampicillin	AMPICILLIN	Medical Purchasing Solutions, LLC	c4310ee5-cbd3-99b5-e053-2995a90ae229	2023-04-27	Warnings, Adverse reactions	Exact identifier rxcui: 1721475 unii: JFN36L5S8K
Ampicillin	AMPICILLIN SODIUM	Fresenius Kabi USA, LLC	8dbb4c71-8543-08f1-e053-2995a90af88d	2022-10-21	Warnings, Adverse reactions	Exact identifier rxcui: 1721474 rxcui: 1721475 rxcui: 1721476 rxcui: 1721473 unii: JFN36L5S8K

Reported adverse events (FAERS/openFDA)#

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