Ampicillin
Ampicillin for Injection, USP
Approved
Approval ID
bbf118c0-7cd3-5a82-e053-2a95a90ac8c8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 8, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ampicillin
PRODUCT DETAILS
NDC Product Code71872-7240
Application NumberANDA062772
Marketing CategoryC73584
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateMay 8, 2023
Generic NameAmpicillin
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 2 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM