Zoledronic Acid

Product NDC

45963-440

11-digit product format

459630440

Labeler code

45963

Product ID

45963-440_a6f44bc4-93d9-44f4-bc52-00ed376f3a7e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Zoledronic Acid

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

Actavis Pharma, Inc.

Application

ANDA202472

Marketing category

ANDA

Marketing start

2015-04-13

Marketing end

2019-05-31

Substance

ZOLEDRONIC ACID

Active strength

4 mg/5mL

Pharmacologic classes

Diphosphonates [CS],Bisphosphonate [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record