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Propylthiouracil - 0143-1480-01 - (Propylthiouracil)

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Drug Information of Propylthiouracil

Product NDC: 0143-1480
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: 0143-1480
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080154
Marketing Category: ANDA
Start Marketing Date: 19710723

Package Information of Propylthiouracil

Package NDC: 0143-1480-01
Package Description: 100 TABLET in 1 BOTTLE (0143-1480-01)

NDC Information of Propylthiouracil

NDC Code 0143-1480-01
Proprietary Name Propylthiouracil
Package Description 100 TABLET in 1 BOTTLE (0143-1480-01)
Product NDC 0143-1480
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propylthiouracil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19710723
Marketing Category Name ANDA
Labeler Name West-ward Pharmaceutical Corp
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


General Information