| NDC Code | 23155-170-31 |
|---|
| Package Description | 1 VIAL, GLASS in 1 CARTON (23155-170-31) / 5 mL in 1 VIAL, GLASS |
|---|
| Product NDC | 23155-170 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Zoledronic Acid |
|---|
| Non-Proprietary Name | Zoledronic Acid |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20230831 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA201783 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
|---|
| Substance Name | ZOLEDRONIC ACID |
|---|
| Strength | 4 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Bisphosphonate [EPC], Diphosphonates [CS] |
|---|