ZOLEDRONIC ACID
- Product NDC
- 0409-4228
- 11-digit product format
- 004094228
- Labeler code
- 0409
- Product ID
- 0409-4228_a3368bb3-b07e-4d46-a5f5-1437b943828c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ZOLEDRONIC ACID
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Hospira, Inc.
- Application
- ANDA202837
- Marketing category
- ANDA
- Marketing start
- 2017-10-19
- Marketing end
- 2022-01-03
- Substance
- ZOLEDRONIC ACID
- Active strength
- 5 mg/100mL
- Pharmacologic classes
- Diphosphonates [CS],Bisphosphonate [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0409-4228-01 | 00409422801 | 1 BAG in 1 CARTON (0409-4228-01) > 100 mL in 1 BAG | 1 bag | 2017-10-19 | 0000-00-00 | No | No | Current |