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Necon 0.5/35 - 52544-550-31 - (Norethindrone and Ethinyl Estradiol Tablets)

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Drug Information of Necon 0.5/35

Product NDC: 52544-550
Proprietary Name: Necon 0.5/35
Non Proprietary Name: Norethindrone and Ethinyl Estradiol Tablets
Active Ingredient(s):    & nbsp;   Norethindrone and Ethinyl Estradiol Tablets
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Necon 0.5/35

Product NDC: 52544-550
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070686
Marketing Category: ANDA
Start Marketing Date: 19870129

Package Information of Necon 0.5/35

Package NDC: 52544-550-31
Package Description: 3 BLISTER PACK in 1 CARTON (52544-550-31) > 1 KIT in 1 BLISTER PACK

NDC Information of Necon 0.5/35

NDC Code 52544-550-31
Proprietary Name Necon 0.5/35
Package Description 3 BLISTER PACK in 1 CARTON (52544-550-31) > 1 KIT in 1 BLISTER PACK
Product NDC 52544-550
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol Tablets
Dosage Form Name KIT
Route Name
Start Marketing Date 19870129
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Necon 0.5/35


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