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Cyclafem 7/7/7 - 0603-7525-17 - (norethindrone and ethinyl estradiol)

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Drug Information of Cyclafem 7/7/7

Product NDC: 0603-7525
Proprietary Name: Cyclafem 7/7/7
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 Cyclafem 7/7/7

Product NDC: 0603-7525
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076338
Marketing Category: ANDA
Start Marketing Date: 20101116

Package Information of Cyclafem 7/7/7

Package NDC: 0603-7525-17
Package Description: 6 BLISTER PACK in 1 CARTON (0603-7525-17) > 1 KIT in 1 BLISTER PACK (0603-7525-01)

NDC Information of Cyclafem 7/7/7

NDC Code 0603-7525-17
Proprietary Name Cyclafem 7/7/7
Package Description 6 BLISTER PACK in 1 CARTON (0603-7525-17) > 1 KIT in 1 BLISTER PACK (0603-7525-01)
Product NDC 0603-7525
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norethindrone and ethinyl estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20101116
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Cyclafem 7/7/7


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