FALMINA - 16714-359-02 - (Levonorgestrel and Ethinyl Estradiol)

Alphabetical Index


Drug Information of FALMINA

Product NDC: 16714-359
Proprietary Name: FALMINA
Non Proprietary Name: Levonorgestrel and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Levonorgestrel and Ethinyl Estradiol
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of FALMINA

Product NDC: 16714-359
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090721
Marketing Category: ANDA
Start Marketing Date: 20120701

Package Information of FALMINA

Package NDC: 16714-359-02
Package Description: 1 BLISTER PACK in 1 CARTON (16714-359-02) > 1 KIT in 1 BLISTER PACK

NDC Information of FALMINA

NDC Code 16714-359-02
Proprietary Name FALMINA
Package Description 1 BLISTER PACK in 1 CARTON (16714-359-02) > 1 KIT in 1 BLISTER PACK
Product NDC 16714-359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levonorgestrel and Ethinyl Estradiol
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20120701
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
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Complete Information of FALMINA


General Information