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Synthroid
Synthroid - 52125-072-02 - (Levothyroxine Sodium)
Drug Information of Synthroid
| Product NDC: | 52125-072 |
| Proprietary Name: | Synthroid |
| Non Proprietary Name: | Levothyroxine Sodium |
| Active Ingredient(s): | 25 ug/1 & nbsp; Levothyroxine Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Synthroid
| Product NDC: | 52125-072 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021402 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130222 |
Package Information of Synthroid
| Package NDC: | 52125-072-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (52125-072-02) |
NDC Information of Synthroid
| NDC Code | 52125-072-02 |
| Proprietary Name | Synthroid |
| Package Description | 30 TABLET in 1 BLISTER PACK (52125-072-02) |
| Product NDC | 52125-072 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levothyroxine Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130222 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | 25 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
