MedPath

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

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0781-3408
Application NumberANDA061395
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
FDA Product Classification

INGREDIENTS (1)

AMPICILLIN SODIUMActive
Quantity: 2 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM

Ampicillin sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0781-3407
Application NumberANDA061395
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
FDA Product Classification

INGREDIENTS (1)

AMPICILLIN SODIUMActive
Quantity: 500 mg in 1 1
Code: JFN36L5S8K
Classification: ACTIM

Ampicillin sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0781-3400
Application NumberANDA061395
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
FDA Product Classification

INGREDIENTS (1)

AMPICILLIN SODIUMActive
Quantity: 125 mg in 1 1
Code: JFN36L5S8K
Classification: ACTIM

Ampicillin sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0781-3404
Application NumberANDA061395
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
FDA Product Classification

INGREDIENTS (1)

AMPICILLIN SODIUMActive
Quantity: 1 g in 1 1
Code: JFN36L5S8K
Classification: ACTIM

Ampicillin sodium

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code0781-3402
Application NumberANDA061395
Product Classification
M
Marketing Category
C73584
G
Generic Name
Ampicillin sodium
Product Specifications
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateOctober 20, 2017
FDA Product Classification

INGREDIENTS (1)

AMPICILLIN SODIUMActive
Quantity: 250 mg in 1 1
Code: JFN36L5S8K
Classification: ACTIM

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