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Azathioprine
Azathioprine - 51079-620-06 - (azathioprine)
Drug Information of Azathioprine
| Product NDC: | 51079-620 |
| Proprietary Name: | Azathioprine |
| Non Proprietary Name: | azathioprine |
| Active Ingredient(s): | 50 mg/1 & nbsp; azathioprine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azathioprine
| Product NDC: | 51079-620 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075568 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110620 |
Package Information of Azathioprine
| Package NDC: | 51079-620-06 |
| Package Description: | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-620-06) > 1 TABLET in 1 BLISTER PACK (51079-620-01) |
NDC Information of Azathioprine
| NDC Code | 51079-620-06 |
| Proprietary Name | Azathioprine |
| Package Description | 50 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-620-06) > 1 TABLET in 1 BLISTER PACK (51079-620-01) |
| Product NDC | 51079-620 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | azathioprine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110620 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | AZATHIOPRINE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Purine Antimetabolite [EPC],Purines [Chemical/Ingredient] |
