Product NDC: | 54868-1093 |
Proprietary Name: | LEVOTHYROXINE SODIUM |
Non Proprietary Name: | Levothyroxine Sodium |
Active Ingredient(s): | .15 mg/1 & nbsp; Levothyroxine Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-1093 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076187 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960924 |
Package NDC: | 54868-1093-2 |
Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (54868-1093-2) |
NDC Code | 54868-1093-2 |
Proprietary Name | LEVOTHYROXINE SODIUM |
Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (54868-1093-2) |
Product NDC | 54868-1093 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Levothyroxine Sodium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19960924 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | LEVOTHYROXINE SODIUM |
Strength Number | .15 |
Strength Unit | mg/1 |
Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |