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Propylthiouracil - 55154-7453-4 - (Propylthiouracil)

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Drug Information of Propylthiouracil

Product NDC: 55154-7453
Proprietary Name: Propylthiouracil
Non Proprietary Name: Propylthiouracil
Active Ingredient(s): 50    mg/1 & nbsp;   Propylthiouracil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Propylthiouracil

Product NDC: 55154-7453
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080154
Marketing Category: ANDA
Start Marketing Date: 19820101

Package Information of Propylthiouracil

Package NDC: 55154-7453-4
Package Description: 100 POUCH in 1 CARTON (55154-7453-4) > 1 TABLET in 1 POUCH (55154-7453-6)

NDC Information of Propylthiouracil

NDC Code 55154-7453-4
Proprietary Name Propylthiouracil
Package Description 100 POUCH in 1 CARTON (55154-7453-4) > 1 TABLET in 1 POUCH (55154-7453-6)
Product NDC 55154-7453
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propylthiouracil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19820101
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name PROPYLTHIOURACIL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Thyroid Hormone Synthesis Inhibitor [EPC],Thyroid Hormone Synthesis Inhibitors [MoA]

Complete Information of Propylthiouracil


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