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The “Company Name” field currently displays the company associated with the drug identification number (DIN) as of today. A fix will be implemented shortly so the fields will show the company name as it was when the report was originally posted. This issue does not impact the data that can be extracted from the website using the Application Programming Interface (API).

Reports for AMPICILLIN

Ingredient

AMPICILLIN

Shortage reports
Brand name	Strength	Dosage	Status	Date Created	Date Updated	Reports
AMPICILLIN SODIUM FOR INJECTION, USP	2G	POWDER FOR SOLUTION	Resolved	2021-07-08	2021-08-24	142189
AMPICILLIN SODIUM FOR INJECTION, USP	2000MG	POWDER FOR SOLUTION	Resolved	2019-06-18	2019-09-19	86942
AMPICILLIN SODIUM FOR INJECTION, USP	1G	POWDER FOR SOLUTION	Resolved	2025-06-05	2025-12-11	259685
AMPICILLIN SODIUM FOR INJECTION, USP	1G	POWDER FOR SOLUTION	Resolved	2022-01-27	2022-12-20	153739
AMPICILLIN SODIUM FOR INJECTION, USP	1G	POWDER FOR SOLUTION	Resolved	2021-06-03	2021-08-05	140369
AMPICILLIN SODIUM FOR INJECTION, USP	1000MG	POWDER FOR SOLUTION	Resolved	2019-06-18	2019-09-19	86939
AMPICILLIN SODIUM FOR INJECTION, USP	500MG	POWDER FOR SOLUTION	Resolved	2025-08-08	2025-12-18	264775
AMPICILLIN SODIUM FOR INJECTION, USP	500MG	POWDER FOR SOLUTION	Resolved	2022-04-28	2023-01-19	159584
AMPICILLIN SODIUM FOR INJECTION, USP	500MG	POWDER FOR SOLUTION	Resolved	2022-03-31	2022-12-20	157650
AMPICILLIN SODIUM FOR INJECTION, USP	500MG	POWDER FOR SOLUTION	Resolved	2021-08-13	2021-10-07	144105

Showing 11 to 20 of 33

Discontinuation reports
Brand name	Strength	Dosage	Status	Date Created	Date Updated	Reports

1

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