Daysee - 68180-846-13 - (LEVONORGESTREL AND ETHINYL ESTRADIOL)

Alphabetical Index


Drug Information of Daysee

Product NDC: 68180-846
Proprietary Name: Daysee
Non Proprietary Name: LEVONORGESTREL AND ETHINYL ESTRADIOL
Active Ingredient(s):    & nbsp;   LEVONORGESTREL AND ETHINYL ESTRADIOL
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Daysee

Product NDC: 68180-846
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091467
Marketing Category: ANDA
Start Marketing Date: 20130410

Package Information of Daysee

Package NDC: 68180-846-13
Package Description: 2 POUCH in 1 CARTON (68180-846-13) > 1 BLISTER PACK in 1 POUCH (68180-846-11) > 1 KIT in 1 BLISTER PACK

NDC Information of Daysee

NDC Code 68180-846-13
Proprietary Name Daysee
Package Description 2 POUCH in 1 CARTON (68180-846-13) > 1 BLISTER PACK in 1 POUCH (68180-846-11) > 1 KIT in 1 BLISTER PACK
Product NDC 68180-846
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEVONORGESTREL AND ETHINYL ESTRADIOL
Dosage Form Name KIT
Route Name
Start Marketing Date 20130410
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Daysee


General Information