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Azathioprine Sodium
Azathioprine Sodium - 55390-600-20 - (Azathioprine Sodium)
Drug Information of Azathioprine Sodium
| Product NDC: | 55390-600 |
| Proprietary Name: | Azathioprine Sodium |
| Non Proprietary Name: | Azathioprine Sodium |
| Active Ingredient(s): | 100 mg/10mL & nbsp; Azathioprine Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azathioprine Sodium
| Product NDC: | 55390-600 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074419 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19950501 |
Package Information of Azathioprine Sodium
| Package NDC: | 55390-600-20 |
| Package Description: | 1 VIAL in 1 BOX, UNIT-DOSE (55390-600-20) > 10 mL in 1 VIAL |
NDC Information of Azathioprine Sodium
| NDC Code | 55390-600-20 |
| Proprietary Name | Azathioprine Sodium |
| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (55390-600-20) > 10 mL in 1 VIAL |
| Product NDC | 55390-600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Azathioprine Sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19950501 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | AZATHIOPRINE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Purine Antimetabolite [EPC],Purines [Chemical/Ingredient] |
