Ampicillin
Ampicillin for Injection, USP
Approved
Approval ID
64a04e8c-8f78-46b3-8f45-56ef225a4f74
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 6, 2020
Manufacturers
FDA
Sandoz Inc
DUNS: 005387188
Products 5
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Ampicillin sodium
PRODUCT DETAILS
NDC Product Code0781-3408
Application NumberANDA061395
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
Generic NameAmpicillin sodium
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 2 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM
Ampicillin sodium
PRODUCT DETAILS
NDC Product Code0781-3407
Application NumberANDA061395
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
Generic NameAmpicillin sodium
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 500 mg in 1 1
Code: JFN36L5S8K
Classification: ACTIM
Ampicillin sodium
PRODUCT DETAILS
NDC Product Code0781-3400
Application NumberANDA061395
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
Generic NameAmpicillin sodium
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 125 mg in 1 1
Code: JFN36L5S8K
Classification: ACTIM
Ampicillin sodium
PRODUCT DETAILS
NDC Product Code0781-3404
Application NumberANDA061395
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
Generic NameAmpicillin sodium
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 1 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM
Ampicillin sodium
PRODUCT DETAILS
NDC Product Code0781-3402
Application NumberANDA061395
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
Generic NameAmpicillin sodium
INGREDIENTS (1)
AMPICILLIN SODIUMActive
Quantity: 250 mg in 1 1
Code: JFN36L5S8K
Classification: ACTIM