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Tri-Norinyl - 52544-274-31 - (Norethindrone and Ethinyl Estradiol)

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Drug Information of Tri-Norinyl

Product NDC: 52544-274
Proprietary Name: Tri-Norinyl
Non Proprietary Name: Norethindrone and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Norethindrone and Ethinyl Estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Tri-Norinyl

Product NDC: 52544-274
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018977
Marketing Category: NDA
Start Marketing Date: 19840413

Package Information of Tri-Norinyl

Package NDC: 52544-274-31
Package Description: 3 BLISTER PACK in 1 CARTON (52544-274-31) > 1 KIT in 1 BLISTER PACK

NDC Information of Tri-Norinyl

NDC Code 52544-274-31
Proprietary Name Tri-Norinyl
Package Description 3 BLISTER PACK in 1 CARTON (52544-274-31) > 1 KIT in 1 BLISTER PACK
Product NDC 52544-274
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 19840413
Marketing Category Name NDA
Labeler Name Watson Pharma, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Tri-Norinyl


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