Zoledronic acid
- Product NDC
- 23155-186
- 11-digit product format
- 231550186
- Labeler code
- 23155
- Product ID
- 23155-186_aa12bee0-bcd3-4ffe-b29d-1d00a7de9ff0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zoledronic acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Heritage Pharmaceuticals Inc.
- Application
- ANDA201801
- Marketing category
- ANDA
- Marketing start
- 2012-12-20
- Marketing end
- 0000-00-00
- Substance
- ZOLEDRONIC ACID
- Active strength
- 5 mg/100mL
- Pharmacologic classes
- Diphosphonates [CS],Bisphosphonate [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record