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LOESTRIN Fe 1.5/30 - 51285-084-98 - (norethindrone acetate and ethinyl estradiol and ferrous fumarate)

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Drug Information of LOESTRIN Fe 1.5/30

Product NDC: 51285-084
Proprietary Name: LOESTRIN Fe 1.5/30
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 LOESTRIN Fe 1.5/30

Product NDC: 51285-084
Labeler Name: Teva Women's Health, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076064
Marketing Category: ANDA
Start Marketing Date: 20081001

Package Information of LOESTRIN Fe 1.5/30

Package NDC: 51285-084-98
Package Description: 30 POUCH in 1 CARTON (51285-084-98) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of LOESTRIN Fe 1.5/30

NDC Code 51285-084-98
Proprietary Name LOESTRIN Fe 1.5/30
Package Description 30 POUCH in 1 CARTON (51285-084-98) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 51285-084
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 20081001
Marketing Category Name ANDA
Labeler Name Teva Women's Health, Inc
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of LOESTRIN Fe 1.5/30


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