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Microgestin Fe - 52544-630-28 - (Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate)

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Drug Information of Microgestin Fe

Product NDC: 52544-630
Proprietary Name: Microgestin Fe
Non Proprietary Name: Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
Active Ingredient(s):    & nbsp;   Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Microgestin Fe

Product NDC: 52544-630
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075647
Marketing Category: ANDA
Start Marketing Date: 20010205

Package Information of Microgestin Fe

Package NDC: 52544-630-28
Package Description: 6 BLISTER PACK in 1 CARTON (52544-630-28) > 1 KIT in 1 BLISTER PACK

NDC Information of Microgestin Fe

NDC Code 52544-630-28
Proprietary Name Microgestin Fe
Package Description 6 BLISTER PACK in 1 CARTON (52544-630-28) > 1 KIT in 1 BLISTER PACK
Product NDC 52544-630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate
Dosage Form Name KIT
Route Name
Start Marketing Date 20010205
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Microgestin Fe


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