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Norethindrone and Ethinyl Estradiol and Ferrous Fumarate - 68180-897-13 - (Norethindrone and Ethinyl Estradiol)

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Drug Information of Norethindrone and Ethinyl Estradiol and Ferrous Fumarate

Product NDC: 68180-897
Proprietary Name: Norethindrone and Ethinyl Estradiol and Ferrous Fumarate
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 Norethindrone and Ethinyl Estradiol and Ferrous Fumarate

Product NDC: 68180-897
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021490
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111004

Package Information of Norethindrone and Ethinyl Estradiol and Ferrous Fumarate

Package NDC: 68180-897-13
Package Description: 5 POUCH in 1 CARTON (68180-897-13) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of Norethindrone and Ethinyl Estradiol and Ferrous Fumarate

NDC Code 68180-897-13
Proprietary Name Norethindrone and Ethinyl Estradiol and Ferrous Fumarate
Package Description 5 POUCH in 1 CARTON (68180-897-13) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 68180-897
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20111004
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Norethindrone and Ethinyl Estradiol and Ferrous Fumarate


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