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Estropipate - 0555-0729-05 - (Estropipate)

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Drug Information of Estropipate

Product NDC: 0555-0729
Proprietary Name: Estropipate
Non Proprietary Name: Estropipate
Active Ingredient(s): 3    mg/1 & nbsp;   Estropipate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Estropipate

Product NDC: 0555-0729
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040135
Marketing Category: ANDA
Start Marketing Date: 19980123

Package Information of Estropipate

Package NDC: 0555-0729-05
Package Description: 1000 TABLET in 1 BOTTLE (0555-0729-05)

NDC Information of Estropipate

NDC Code 0555-0729-05
Proprietary Name Estropipate
Package Description 1000 TABLET in 1 BOTTLE (0555-0729-05)
Product NDC 0555-0729
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estropipate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980123
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name ESTROPIPATE
Strength Number 3
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Estropipate


General Information