Ampicillin sodium
Ampicillin for Injection, USP
Approved
Approval ID
34e95c91-3767-493c-8716-38e61e7c6674
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 10, 2023
Manufacturers
FDA
Armas Pharmaceuticals Inc.
DUNS: 098405973
Products 2
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ampicillin Sodium
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72485-422
Application NumberANDA201025
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin Sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateNovember 10, 2023
FDA Product Classification
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 2 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM
Ampicillin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code72485-421
Application NumberANDA201025
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateNovember 10, 2023
FDA Product Classification
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 1 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM