Desoxyn - 67386-102-01 - (methamphetamine hydrochloride)

Alphabetical Index


Drug Information of Desoxyn

Product NDC: 67386-102
Proprietary Name: Desoxyn
Non Proprietary Name: methamphetamine hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   methamphetamine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Desoxyn

Product NDC: 67386-102
Labeler Name: Lundbeck Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA005378
Marketing Category: NDA
Start Marketing Date: 19431231

Package Information of Desoxyn

Package NDC: 67386-102-01
Package Description: 100 TABLET in 1 BOTTLE (67386-102-01)

NDC Information of Desoxyn

NDC Code 67386-102-01
Proprietary Name Desoxyn
Package Description 100 TABLET in 1 BOTTLE (67386-102-01)
Product NDC 67386-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methamphetamine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19431231
Marketing Category Name NDA
Labeler Name Lundbeck Inc.
Substance Name METHAMPHETAMINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Amphetamine Anorectic [EPC],Amphetamines [Chemical/Ingredient],Appetite Suppression [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE]

Complete Information of Desoxyn


General Information