Ceftazidime

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 829274633

Effective Date

September 23, 2021

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

Ceftazidime(6 g in 100 mL)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

44567-237

Application Number

ANDA062640

Marketing Category

ANDA (C73584)

Route of Administration

INTRAVENOUS

Effective Date

September 1, 2021

Ingredients

Code: 9M416Z9QNRClass: ACTIMQuantity: 6 g in 100 mL

natural latex rubberInactive

Code: 2LQ0UUW8INClass: CNTMQuantity: 0 1 in 100 mL