Home > National Drug Code (NDC) > Junel Fe 1/20

Junel Fe 1/20 - 0555-9026-58 - (norethindrone acetate and ethinyl estradiol, and ferrous fumarate)

Alphabetical Index


Drug Information of Junel Fe 1/20

Product NDC: 0555-9026
Proprietary Name: Junel Fe 1/20
Non Proprietary Name: norethindrone acetate and ethinyl estradiol, and ferrous fumarate
Active Ingredient(s):    & nbsp;   norethindrone acetate and ethinyl estradiol, and ferrous fumarate
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Junel Fe 1/20

Product NDC: 0555-9026
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076081
Marketing Category: ANDA
Start Marketing Date: 20030918

Package Information of Junel Fe 1/20

Package NDC: 0555-9026-58
Package Description: 6 BLISTER PACK in 1 CARTON (0555-9026-58) > 1 KIT in 1 BLISTER PACK

NDC Information of Junel Fe 1/20

NDC Code 0555-9026-58
Proprietary Name Junel Fe 1/20
Package Description 6 BLISTER PACK in 1 CARTON (0555-9026-58) > 1 KIT in 1 BLISTER PACK
Product NDC 0555-9026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name norethindrone acetate and ethinyl estradiol, and ferrous fumarate
Dosage Form Name KIT
Route Name
Start Marketing Date 20030918
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Junel Fe 1/20


General Information