Zoledronic acid
- Product NDC
- 67457-920
- 11-digit product format
- 674570920
- Labeler code
- 67457
- Product ID
- 67457-920_bd74d695-4592-4372-aaa7-2b7fa188c1b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zoledronic acid
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Mylan Institutional LLC
- Application
- ANDA202650
- Marketing category
- ANDA
- Marketing start
- 2020-10-12
- Marketing end
- 0000-00-00
- Substance
- ZOLEDRONIC ACID
- Active strength
- 4 mg/5mL
- Pharmacologic classes
- Bisphosphonate [EPC], Diphosphonates [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67457-920-05 | 67457092005 | 1 VIAL in 1 CARTON (67457-920-05) > 5 mL in 1 VIAL | 1 vial | 2020-10-12 | 0000-00-00 | No | No | Current |