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Norgestrel/Ethinyl Estradiol - 24090-961-84 - (norgestrel/ethinyl estradiol)

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Drug Information of Norgestrel/Ethinyl Estradiol

Product NDC: 24090-961
Proprietary Name: Norgestrel/Ethinyl Estradiol
Non Proprietary Name: norgestrel/ethinyl estradiol
Active Ingredient(s):    & nbsp;   norgestrel/ethinyl estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Norgestrel/Ethinyl Estradiol

Product NDC: 24090-961
Labeler Name: Akrimax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017802
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19760301

Package Information of Norgestrel/Ethinyl Estradiol

Package NDC: 24090-961-84
Package Description: 6 BLISTER PACK in 1 CARTON (24090-961-84) > 1 KIT in 1 BLISTER PACK

NDC Information of Norgestrel/Ethinyl Estradiol

NDC Code 24090-961-84
Proprietary Name Norgestrel/Ethinyl Estradiol
Package Description 6 BLISTER PACK in 1 CARTON (24090-961-84) > 1 KIT in 1 BLISTER PACK
Product NDC 24090-961
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norgestrel/ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 19760301
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Akrimax Pharmaceuticals, LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Norgestrel/Ethinyl Estradiol


General Information