Velivet - 0555-9051-67 - (Desogestrel and Ethinyl Estradiol)

Alphabetical Index


Drug Information of Velivet

Product NDC: 0555-9051
Proprietary Name: Velivet
Non Proprietary Name: Desogestrel and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Desogestrel and Ethinyl Estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Velivet

Product NDC: 0555-9051
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076455
Marketing Category: ANDA
Start Marketing Date: 20040301

Package Information of Velivet

Package NDC: 0555-9051-67
Package Description: 3 POUCH in 1 CARTON (0555-9051-67) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK

NDC Information of Velivet

NDC Code 0555-9051-67
Proprietary Name Velivet
Package Description 3 POUCH in 1 CARTON (0555-9051-67) > 1 BLISTER PACK in 1 POUCH > 1 KIT in 1 BLISTER PACK
Product NDC 0555-9051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desogestrel and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 20040301
Marketing Category Name ANDA
Labeler Name Barr Laboratories Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Velivet


General Information