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Levothyroxine Sodium
Levothyroxine Sodium - 49349-334-20 - (Levothyroxine Sodium)
Drug Information of Levothyroxine Sodium
| Product NDC: | 49349-334 |
| Proprietary Name: | Levothyroxine Sodium |
| Non Proprietary Name: | Levothyroxine Sodium |
| Active Ingredient(s): | .075 mg/1 & nbsp; Levothyroxine Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levothyroxine Sodium
| Product NDC: | 49349-334 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076752 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110627 |
Package Information of Levothyroxine Sodium
| Package NDC: | 49349-334-20 |
| Package Description: | 100 TABLET in 1 CANISTER (49349-334-20) |
NDC Information of Levothyroxine Sodium
| NDC Code | 49349-334-20 |
| Proprietary Name | Levothyroxine Sodium |
| Package Description | 100 TABLET in 1 CANISTER (49349-334-20) |
| Product NDC | 49349-334 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Levothyroxine Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110627 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | .075 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
