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GILDESS FE 1.5/30 - 0603-7608-17 - (norethindrone acetate, ethinyl estradiol and ferrous fumarate)

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Drug Information of GILDESS FE 1.5/30

Product NDC: 0603-7608
Proprietary Name: GILDESS FE 1.5/30
Non Proprietary Name: norethindrone acetate, ethinyl estradiol and ferrous fumarate
Active Ingredient(s):    & nbsp;   norethindrone acetate, ethinyl estradiol and ferrous fumarate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of GILDESS FE 1.5/30

Product NDC: 0603-7608
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077075
Marketing Category: ANDA
Start Marketing Date: 20050428

Package Information of GILDESS FE 1.5/30

Package NDC: 0603-7608-17
Package Description: 6 BLISTER PACK in 1 CARTON (0603-7608-17) > 1 KIT in 1 BLISTER PACK (0603-7608-01)

NDC Information of GILDESS FE 1.5/30

NDC Code 0603-7608-17
Proprietary Name GILDESS FE 1.5/30
Package Description 6 BLISTER PACK in 1 CARTON (0603-7608-17) > 1 KIT in 1 BLISTER PACK (0603-7608-01)
Product NDC 0603-7608
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norethindrone acetate, ethinyl estradiol and ferrous fumarate
Dosage Form Name KIT
Route Name
Start Marketing Date 20050428
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of GILDESS FE 1.5/30


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