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Pentasa
Pentasa - 49349-561-21 - (Mesalamine)
Drug Information of Pentasa
| Product NDC: | 49349-561 |
| Proprietary Name: | Pentasa |
| Non Proprietary Name: | Mesalamine |
| Active Ingredient(s): | 500 mg/1 & nbsp; Mesalamine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pentasa
| Product NDC: | 49349-561 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020049 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111004 |
Package Information of Pentasa
| Package NDC: | 49349-561-21 |
| Package Description: | 120 CAPSULE in 1 CANISTER (49349-561-21) |
NDC Information of Pentasa
| NDC Code | 49349-561-21 |
| Proprietary Name | Pentasa |
| Package Description | 120 CAPSULE in 1 CANISTER (49349-561-21) |
| Product NDC | 49349-561 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Mesalamine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20111004 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | MESALAMINE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aminosalicylate [EPC],Aminosalicylic Acids [Chemical/Ingredient] |
