Zoledronic Acid

Product NDC
42023-163
11-digit product format
420230163
Labeler code
42023
Product ID
42023-163_10f01dec-5af0-4b0d-bd58-432954914daa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zoledronic Acid
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Par Pharmaceutical Companies, Inc.
Application
ANDA202163
Marketing category
ANDA
Marketing start
2013-08-05
Marketing end
0000-00-00
Substance
ZOLEDRONIC ACID
Active strength
5 mg/100mL
Pharmacologic classes
Diphosphonates [CS],Bisphosphonate [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42023-163-012020-03-12C16284748780-19d75b9d0-f253-f424-e053-dadaa90a57ce9da5186d-a292-4895-aa7d-1ca20c972ae5
42023-163-012020-01-31C16284748780-19d75b9d0-f253-f424-e053-dadaa90a57ce9da5186d-a292-4895-aa7d-1ca20c972ae5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42023-163-01ML - Milliliter42023-163bd19a009-f3dd-437b-91b9-24ad05c48f7712014-01-04