Zoledronic Acid

Product NDC

42023-151

11-digit product format

420230151

Labeler code

42023

Product ID

42023-151_4542c741-e291-4488-969e-a86d2f9e2ce9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Zoledronic Acid

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Par Pharmaceutical Companies, Inc.

Application

ANDA091170

Marketing category

ANDA

Marketing start

2013-03-04

Marketing end

0000-00-00

Substance

ZOLEDRONIC ACID

Active strength

4 mg/5mL

Pharmacologic classes

Diphosphonates [CS],Bisphosphonate [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record