Zometa

Product NDC

0078-0590

11-digit product format

000780590

Labeler code

0078

Product ID

0078-0590_f7adde0d-fe18-4171-b804-64479f171814

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

zoledronic acid

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Novartis Pharmaceuticals Corporation

Application

NDA021223

Marketing category

NDA

Marketing start

2001-08-20

Marketing end

2020-01-31

Substance

ZOLEDRONIC ACID

Active strength

4 mg/100mL

Pharmacologic classes

Diphosphonates [CS],Bisphosphonate [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record