zoledronic acid
- Product NDC
- 50742-416
- 11-digit product format
- 507420416
- Labeler code
- 50742
- Product ID
- 50742-416_c7a5297d-f017-46f8-895b-7187ef93ce09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- zoledronic acid
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA208968
- Marketing category
- ANDA
- Marketing start
- 2020-02-19
- Marketing end
- 0000-00-00
- Substance
- ZOLEDRONIC ACID
- Active strength
- 4 mg/5mL
- Pharmacologic classes
- Diphosphonates [CS],Bisphosphonate [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 50742-416-05 | 50742041605 | 1 VIAL in 1 CARTON (50742-416-05) > 5 mL in 1 VIAL | 1 vial | 2020-02-19 | 0000-00-00 | No | No | Current |