NDC 72572-021-01 - Ampicillin and Sulbactam

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: 72572-021
Requested NDC: 72572-021-01
Package NDCs from labels: 72572-021-01, 72572-021-10
Manufacturer: Civica, Inc.
Effective date: 2022-12-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ampicillin and Sulbactam - Civica, Inc.	Civica, Inc.	2022-12-15	Human Prescription Drug Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72572-021-10	2024-01-30	C162847	48780-1	1030e365-488d-111a-e063-dadaa90a10e2	Ampicillin and Sulbactam for Injection, USP (For Intramuscular or Intravenous Use)

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72572-021-01	EA - Each	72572-021	5a21143e-787b-430f-8026-c928b2708bbe	1	2022-03-09
72572-021-10	EA - Each	72572-021	cb7bedbf-a74e-48a6-85b5-da83bcf45d87	1	2022-03-09

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 · 63 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ampicillin	AMPICILLIN	Medical Purchasing Solutions, LLC	bbf118c0-7cd3-5a82-e053-2a95a90ac8c8	2023-05-08	Warnings, Adverse reactions	Exact identifier unii: JFN36L5S8K
Ampicillin	AMPICILLIN	Medical Purchasing Solutions, LLC	c4310ee5-cbd3-99b5-e053-2995a90ae229	2023-04-27	Warnings, Adverse reactions	Exact identifier unii: JFN36L5S8K
Ampicillin	AMPICILLIN SODIUM	Fresenius Kabi USA, LLC	8dbb4c71-8543-08f1-e053-2995a90af88d	2022-10-21	Warnings, Adverse reactions	Exact identifier unii: JFN36L5S8K

Reported adverse events (FAERS/openFDA)#

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