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Tirosint
Tirosint - 24090-495-07 - (Levothyroxine Sodium)
Drug Information of Tirosint
| Product NDC: | 24090-495 |
| Proprietary Name: | Tirosint |
| Non Proprietary Name: | Levothyroxine Sodium |
| Active Ingredient(s): | 100 ug/1 & nbsp; Levothyroxine Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tirosint
| Product NDC: | 24090-495 |
| Labeler Name: | Akrimax Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021924 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100401 |
Package Information of Tirosint
| Package NDC: | 24090-495-07 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (24090-495-07) > 7 CAPSULE in 1 BLISTER PACK |
NDC Information of Tirosint
| NDC Code | 24090-495-07 |
| Proprietary Name | Tirosint |
| Package Description | 1 BLISTER PACK in 1 CARTON (24090-495-07) > 7 CAPSULE in 1 BLISTER PACK |
| Product NDC | 24090-495 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levothyroxine Sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100401 |
| Marketing Category Name | NDA |
| Labeler Name | Akrimax Pharmaceuticals, LLC |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | 100 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
