NDC 51662-1595-2 - 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: 51662-1595
Requested NDC: 51662-1595-2
Package NDCs from labels: 51662-1595-2, 51662-1595-3
Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Effective date: 2024-01-28
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
AMPICILLIN - HF Acquisition Co LLC, DBA HealthFirst	HF Acquisition Co LLC, DBA HealthFirst	2024-01-28	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51662-1595-2	AMPICILLIN	1 in 1 POUCH	INJECTION, POWDER, FOR SOLUTION	1	3
51662-1595-2	AMPICILLIN	1 in 1 VIAL	INJECTION, POWDER, FOR SOLUTION	1	3
51662-1595-3	AMPICILLIN	10 in 1 CASE	INJECTION, POWDER, FOR SOLUTION	10	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51662-1595	AMPICILLIN INJECTION, POWDER, FOR SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]	3	Current NDC, Legacy NDC, 3 package rows	20240130_e47a21b1-bbdb-4321-e053-2a95a90a3b4a.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 application number: ANDA062719 ndc (product): 65219-014 rxcui: 1721474 rxcui: 1721475 rxcui: 1721476 rxcui: 1721473 spl id: 38c6c088-e4ab-4859-b4d9-89e846cf9d5f spl set id: 8dbb4c71-8543-08f1-e053-2995a90af88d unii: JFN36L5S8K

Reported adverse events (FAERS/openFDA)#

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