Androgel - 0051-8462-31 - (Testosterone)

Alphabetical Index


Drug Information of Androgel

Product NDC: 0051-8462
Proprietary Name: Androgel
Non Proprietary Name: Testosterone
Active Ingredient(s): 16.2    mg/g & nbsp;   Testosterone
Administration Route(s): TRANSDERMAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Androgel

Product NDC: 0051-8462
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022309
Marketing Category: NDA
Start Marketing Date: 20110429

Package Information of Androgel

Package NDC: 0051-8462-31
Package Description: 30 PACKET in 1 CARTON (0051-8462-31) > 1.25 g in 1 PACKET (0051-8462-12)

NDC Information of Androgel

NDC Code 0051-8462-31
Proprietary Name Androgel
Package Description 30 PACKET in 1 CARTON (0051-8462-31) > 1.25 g in 1 PACKET (0051-8462-12)
Product NDC 0051-8462
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Testosterone
Dosage Form Name GEL
Route Name TRANSDERMAL
Start Marketing Date 20110429
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name TESTOSTERONE
Strength Number 16.2
Strength Unit mg/g
Pharmaceutical Classes Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient]

Complete Information of Androgel


General Information