Myzilra - 0603-7625-17 - (Levonorgestrel and Ethinyl Estradiol)

Alphabetical Index


Drug Information of Myzilra

Product NDC: 0603-7625
Proprietary Name: Myzilra
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 Myzilra

Product NDC: 0603-7625
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077502
Marketing Category: ANDA
Start Marketing Date: 20120112

Package Information of Myzilra

Package NDC: 0603-7625-17
Package Description: 6 BLISTER PACK in 1 CARTON (0603-7625-17) > 1 KIT in 1 BLISTER PACK (0603-7625-01)

NDC Information of Myzilra

NDC Code 0603-7625-17
Proprietary Name Myzilra
Package Description 6 BLISTER PACK in 1 CARTON (0603-7625-17) > 1 KIT in 1 BLISTER PACK (0603-7625-01)
Product NDC 0603-7625
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levonorgestrel and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20120112
Marketing Category Name ANDA
Labeler Name Qualitest Pharmaceuticals
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Myzilra


General Information