Zoledronic Acid

Product NDC
42023-167
11-digit product format
420230167
Labeler code
42023
Product ID
42023-167_7133e3cf-682e-4098-867b-66a9185e5c88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Zoledronic Acid
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Labeler
JHP Pharmaceuticals, LLC.
Application
ANDA202571
Marketing category
ANDA
Marketing start
2013-05-07
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42023-167-012020-03-18C16284748780-19855d018-e696-cd31-e053-dbdaa90ab51a006aec5c-3ea9-4a5e-b912-535f6ca0b690
42023-167-012019-11-27C16284748780-19855d018-e696-cd31-e053-dbdaa90ab51a006aec5c-3ea9-4a5e-b912-535f6ca0b690