Zoledronic Acid
- Product NDC
- 55111-688
- 11-digit product format
- 551110688
- Labeler code
- 55111
- Product ID
- 55111-688_251add88-5c4f-2750-c713-744fcf3a60ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zoledronic Acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Dr.Reddy's Laboratories Ltd
- Application
- ANDA091363
- Marketing category
- ANDA
- Marketing start
- 2013-04-03
- Substance
- ZOLEDRONIC ACID
- Active strength
- 5 mg/100mL
- Pharmacologic classes
- Bisphosphonate [EPC], Diphosphonates [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zoledronic Acid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZOLEDRONIC ACID | 5 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6XC1PAD3KF |
| Rxcui | 705824 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55111-688-52 | Zoledronic Acid | 100 mL in 1 BOTTLE, GLASS | INJECTION, SOLUTION | 100 | | 20 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55111-688 | ZOLEDRONIC ACID (ZOLEDRONIC ACID ) INJECTION, SOLUTION [DR.REDDY'S LABORATORIES LTD] | 20 | Current NDC, Legacy NDC, 1 package rows | 20250117_f94a5c9e-74bc-d09e-cd65-394b2a5de2ad.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55111-688-52 | 55111068852 | 100 mL in 1 BOTTLE, GLASS (55111-688-52) | 100 ml | 2013-04-03 | 0000-00-00 | No | No | Current |