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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71872-7240
Application NumberANDA062772
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateMay 8, 2023
FDA Product Classification
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 2 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM