NDC 71872-7332-01 - 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: 71872-7332
Requested NDC: 71872-7332-01
Package NDCs from labels: 71872-7332-1, 71872-7332-01
Manufacturer: Medical Purchasing Solutions, LLC
Effective date: 2024-12-16
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ampicillin - Medical Purchasing Solutions, LLC	Medical Purchasing Solutions, LLC	2024-12-16	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71872-7332-1	Ampicillin	1 in 1 VIAL	INJECTION, POWDER, FOR SOLUTION	1		1
71872-7332-1	Ampicillin	1 in 1 BAG	INJECTION, POWDER, FOR SOLUTION	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71872-7332	AMPICILLIN INJECTION, POWDER, FOR SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC]	1	Current NDC, 2 package rows	20241218_29675d9c-3248-337a-e063-6294a90a2e20.zip

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: 1721475 rxcui: 1721476 unii: JFN36L5S8K

Reported adverse events (FAERS/openFDA)#

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