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Estropipate - 0591-0414-05 - (Estropipate)

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Drug Information of Estropipate

Product NDC: 0591-0414
Proprietary Name: Estropipate
Non Proprietary Name: Estropipate
Active Ingredient(s): .75    mg/1 & nbsp;   Estropipate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Estropipate

Product NDC: 0591-0414
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081213
Marketing Category: ANDA
Start Marketing Date: 19930923

Package Information of Estropipate

Package NDC: 0591-0414-05
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (0591-0414-05)

NDC Information of Estropipate

NDC Code 0591-0414-05
Proprietary Name Estropipate
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (0591-0414-05)
Product NDC 0591-0414
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Estropipate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19930923
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name ESTROPIPATE
Strength Number .75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Estropipate


General Information