Zoledronic Acid
- Product NDC
- 70860-210
- 11-digit product format
- 708600210
- Labeler code
- 70860
- Product ID
- 70860-210_57894a8f-0e43-4882-80cf-d2e61598ce56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zoledronic acid
- Dosage form
- SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA205749
- Marketing category
- ANDA
- Marketing start
- 2018-12-01
- Marketing end
- 0000-00-00
- Substance
- ZOLEDRONIC ACID
- Active strength
- 4 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-210-51 | 70860021051 | 1 VIAL, SINGLE-USE in 1 CARTON (70860-210-51) > 100 mL in 1 VIAL, SINGLE-USE | 2019-03-13 | 0000-00-00 | No | No | Current |