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Levothyroxine Sodium - 43063-421-30 - (Levothyroxine Sodium)

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Drug Information of Levothyroxine Sodium

Product NDC: 43063-421
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: 43063-421
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021210
Marketing Category: NDA
Start Marketing Date: 20031201

Package Information of Levothyroxine Sodium

Package NDC: 43063-421-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (43063-421-30)

NDC Information of Levothyroxine Sodium

NDC Code 43063-421-30
Proprietary Name Levothyroxine Sodium
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (43063-421-30)
Product NDC 43063-421
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levothyroxine Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031201
Marketing Category Name NDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name LEVOTHYROXINE SODIUM
Strength Number .075
Strength Unit mg/1
Pharmaceutical Classes l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]

Complete Information of Levothyroxine Sodium


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