| NDC Code | 55390-600-20 |
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| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (55390-600-20) > 10 mL in 1 VIAL |
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| Product NDC | 55390-600 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Azathioprine Sodium |
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| Non-Proprietary Name | Azathioprine Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 19950501 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA074419 |
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| Manufacturer | Bedford Laboratories |
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| Substance Name | AZATHIOPRINE SODIUM |
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| Strength | 100 |
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| Strength Unit | mg/10mL |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Purine Antimetabolite [EPC],Purines [Chemical/Ingredient] |
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