| NDC Code | 51991-065-97 |
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| Package Description | 1 VIAL, GLASS in 1 CARTON (51991-065-97) > 5 mL in 1 VIAL, GLASS |
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| Product NDC | 51991-065 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zoledronic Acid |
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| Non-Proprietary Name | Zoledronic Acid |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20200501 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202571 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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| Substance Name | ZOLEDRONIC ACID |
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| Strength | 4 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Diphosphonates [CS],Bisphosphonate [EPC] |
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