LEVONEST - 34908-620-51 - (levonorgestrel and ethinyl estradiol)

Alphabetical Index


Drug Information of LEVONEST

Product NDC: 34908-620
Proprietary Name: LEVONEST
Non Proprietary Name: levonorgestrel and ethinyl estradiol
Active Ingredient(s):    & nbsp;   levonorgestrel and ethinyl estradiol
Administration Route(s): ORAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of LEVONEST

Product NDC: 34908-620
Labeler Name: Novast Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090719
Marketing Category: ANDA
Start Marketing Date: 20110331

Package Information of LEVONEST

Package NDC: 34908-620-51
Package Description: 1 BLISTER PACK in 1 CARTON (34908-620-51) > 1 KIT in 1 BLISTER PACK

NDC Information of LEVONEST

NDC Code 34908-620-51
Proprietary Name LEVONEST
Package Description 1 BLISTER PACK in 1 CARTON (34908-620-51) > 1 KIT in 1 BLISTER PACK
Product NDC 34908-620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levonorgestrel and ethinyl estradiol
Dosage Form Name KIT
Route Name ORAL
Start Marketing Date 20110331
Marketing Category Name ANDA
Labeler Name Novast Laboratories, Ltd.
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Complete Information of LEVONEST


General Information