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Mercaptopurine
Mercaptopurine - 49349-606-16 - (Mercaptopurine)
Drug Information of Mercaptopurine
| Product NDC: | 49349-606 |
| Proprietary Name: | Mercaptopurine |
| Non Proprietary Name: | Mercaptopurine |
| Active Ingredient(s): | 50 mg/1 & nbsp; Mercaptopurine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mercaptopurine
| Product NDC: | 49349-606 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040528 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111103 |
Package Information of Mercaptopurine
| Package NDC: | 49349-606-16 |
| Package Description: | 50 TABLET in 1 CANISTER (49349-606-16) |
NDC Information of Mercaptopurine
| NDC Code | 49349-606-16 |
| Proprietary Name | Mercaptopurine |
| Package Description | 50 TABLET in 1 CANISTER (49349-606-16) |
| Product NDC | 49349-606 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mercaptopurine |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111103 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | MERCAPTOPURINE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
