Necon - 21695-857-01 - (Norethindrone and Ethinyl Estradiol)

Alphabetical Index


Drug Information of Necon

Product NDC: 21695-857
Proprietary Name: Necon
Non Proprietary Name: Norethindrone and Ethinyl Estradiol
Active Ingredient(s):    & nbsp;   Norethindrone and Ethinyl Estradiol
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Necon

Product NDC: 21695-857
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070687
Marketing Category: ANDA
Start Marketing Date: 19870129

Package Information of Necon

Package NDC: 21695-857-01
Package Description: 6 BLISTER PACK in 1 CARTON (21695-857-01) > 1 KIT in 1 BLISTER PACK

NDC Information of Necon

NDC Code 21695-857-01
Proprietary Name Necon
Package Description 6 BLISTER PACK in 1 CARTON (21695-857-01) > 1 KIT in 1 BLISTER PACK
Product NDC 21695-857
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone and Ethinyl Estradiol
Dosage Form Name KIT
Route Name
Start Marketing Date 19870129
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Necon


General Information