AMPICILLIN (AMPICILLIN SODIUM)
Summary
FDA approved AMPICILLIN (AMPICILLIN SODIUM) by EUGIA PHARMA SPECLTS. ANDA (Generic) approval (Labeling) on 2024-05-01. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA065499-13
Action Date
2024-05-01
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
AMPICILLIN (generic: AMPICILLIN SODIUM), INJECTABLE, INJECTION. Application: ANDA065499
Company
Context & Analysis
EUGIA PHARMA SPECLTS has 4 FDA actions in our database.
Frequently Asked Questions
How often does EUGIA PHARMA SPECLTS have FDA actions?
EUGIA PHARMA SPECLTS has 4 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA065499-13" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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