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Ogestrel 0.5/50 - 52544-848-28 - (Norgestrel and Ethinyl Estradiol Tablets)

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Drug Information of Ogestrel 0.5/50

Product NDC: 52544-848
Proprietary Name: Ogestrel 0.5/50
Non Proprietary Name: Norgestrel and Ethinyl Estradiol Tablets
Active Ingredient(s):    & nbsp;   Norgestrel and Ethinyl Estradiol Tablets
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Ogestrel 0.5/50

Product NDC: 52544-848
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075406
Marketing Category: ANDA
Start Marketing Date: 19991215

Package Information of Ogestrel 0.5/50

Package NDC: 52544-848-28
Package Description: 3 BLISTER PACK in 1 CARTON (52544-848-28) > 1 KIT in 1 BLISTER PACK

NDC Information of Ogestrel 0.5/50

NDC Code 52544-848-28
Proprietary Name Ogestrel 0.5/50
Package Description 3 BLISTER PACK in 1 CARTON (52544-848-28) > 1 KIT in 1 BLISTER PACK
Product NDC 52544-848
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norgestrel and Ethinyl Estradiol Tablets
Dosage Form Name KIT
Route Name
Start Marketing Date 19991215
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Ogestrel 0.5/50


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