Zoledronic Acid
- Product NDC
- 70860-802
- 11-digit product format
- 708600802
- Labeler code
- 70860
- Product ID
- 70860-802_4d7afc49-1611-4754-aed4-99a47334f9b0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zoledronic acid
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA209578
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- 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
- 2022-12-31
- 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 |
|---|
| 70860-802-82 | 70860080282 | 1 BAG in 1 CARTON (70860-802-82) > 100 mL in 1 BAG | 1 bag | 2019-09-30 | 0000-00-00 | No | No | Current |