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