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#