ZOLEDRONIC ACID
- Product NDC
- 69097-399
- 11-digit product format
- 690970399
- Labeler code
- 69097
- Product ID
- 69097-399_cf930dec-41f6-4cdf-8938-9244258d2c1e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ZOLEDRONIC ACID
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Cipla USA Inc.
- Application
- ANDA210174
- Marketing category
- ANDA
- Marketing start
- 2017-10-27
- 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