IMPLANON - 0052-0272-01 - (etonogestrel)

Alphabetical Index


Drug Information of IMPLANON

Product NDC: 0052-0272
Proprietary Name: IMPLANON
Non Proprietary Name: etonogestrel
Active Ingredient(s): 68    mg/1 & nbsp;   etonogestrel
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): IMPLANT
Coding System: National Drug Codes(NDC)

Labeler Information of IMPLANON

Product NDC: 0052-0272
Labeler Name: Organon Pharmaceuticals USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021529
Marketing Category: NDA
Start Marketing Date: 20110906

Package Information of IMPLANON

Package NDC: 0052-0272-01
Package Description: 1 BLISTER PACK in 1 CARTON (0052-0272-01) > 1 IMPLANT in 1 BLISTER PACK

NDC Information of IMPLANON

NDC Code 0052-0272-01
Proprietary Name IMPLANON
Package Description 1 BLISTER PACK in 1 CARTON (0052-0272-01) > 1 IMPLANT in 1 BLISTER PACK
Product NDC 0052-0272
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name etonogestrel
Dosage Form Name IMPLANT
Route Name SUBCUTANEOUS
Start Marketing Date 20110906
Marketing Category Name NDA
Labeler Name Organon Pharmaceuticals USA
Substance Name ETONOGESTREL
Strength Number 68
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of IMPLANON


General Information