Home > National Drug Code (NDC) > Propylthiouracil

Propylthiouracil - 24236-204-20 - (Propylthiouracil)

Alphabetical Index


Drug Information of Propylthiouracil

Product NDC: 24236-204
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: 24236-204
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080154
Marketing Category: ANDA
Start Marketing Date: 20130320

Package Information of Propylthiouracil

Package NDC: 24236-204-20
Package Description: 100 TABLET in 1 CANISTER (24236-204-20)

NDC Information of Propylthiouracil

NDC Code 24236-204-20
Proprietary Name Propylthiouracil
Package Description 100 TABLET in 1 CANISTER (24236-204-20)
Product NDC 24236-204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Propylthiouracil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130320
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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