Zoledronic Acid
- Product NDC
- 17478-324
- 11-digit product format
- 174780324
- Labeler code
- 17478
- Product ID
- 17478-324_78e7f4a3-fa27-4aa8-88ed-3a4d89724328
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zoledronic Acid
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA200918
- Marketing category
- ANDA
- Marketing start
- 2014-08-21
- Marketing end
- 0000-00-00
- Substance
- ZOLEDRONIC ACID
- Active strength
- 5 mg/100mL
- Pharmacologic classes
- Bisphosphonate [EPC], Diphosphonates [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 17478-324-91 | 17478032491 | 1 BAG in 1 CARTON (17478-324-91) > 100 mL in 1 BAG | 1 bag | 2014-08-21 | 0000-00-00 | No | No | Current |