ELINEST - 16714-365-03 - (Norgestrel and Ethinyl Estradiol)

Alphabetical Index


Drug Information of ELINEST

Product NDC: 16714-365
Proprietary Name: ELINEST
Non Proprietary Name: Norgestrel and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Norgestrel and Ethinyl Estradiol
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of ELINEST

Product NDC: 16714-365
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091105
Marketing Category: ANDA
Start Marketing Date: 20120701

Package Information of ELINEST

Package NDC: 16714-365-03
Package Description: 3 BLISTER PACK in 1 CARTON (16714-365-03) > 1 KIT in 1 BLISTER PACK

NDC Information of ELINEST

NDC Code 16714-365-03
Proprietary Name ELINEST
Package Description 3 BLISTER PACK in 1 CARTON (16714-365-03) > 1 KIT in 1 BLISTER PACK
Product NDC 16714-365
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norgestrel and Ethinyl Estradiol
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20120701
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name
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Complete Information of ELINEST


General Information