| NDC Code | 47335-932-44 |
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| Package Description | 10 VIAL in 1 BOX (47335-932-44) > 20 mL in 1 VIAL (47335-932-40) |
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| Product NDC | 47335-932 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Vecuronium Bromide |
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| Non-Proprietary Name | Vecuronium Bromide |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20141215 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079001 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | VECURONIUM BROMIDE |
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| Strength | 1 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Neuromuscular Nondepolarizing Blockade [PE], Nondepolarizing Neuromuscular Blocker [EPC] |
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