Cefazolin

Product NDC

0781-9338

11-digit product format

007819338

Labeler code

0781

Product ID

0781-9338_6905adf3-d1e7-4871-b19e-6605c9e17b13

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefazolin

Dosage form

INJECTION, POWDER, FOR SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS; PARENTERAL

Labeler

Sandoz Inc

Application

ANDA062831

Marketing category

ANDA

Marketing start

1988-12-09

Marketing end

2019-06-30

Substance

CEFAZOLIN SODIUM

Active strength

500 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record