Product NDC: | 54569-6187 |
Proprietary Name: | Alprazolam |
Non Proprietary Name: | alprazolam |
Active Ingredient(s): | 1 mg/1 & nbsp; alprazolam |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-6187 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077391 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110504 |
Package NDC: | 54569-6187-0 |
Package Description: | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54569-6187-0) |
NDC Code | 54569-6187-0 |
Proprietary Name | Alprazolam |
Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54569-6187-0) |
Product NDC | 54569-6187 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | alprazolam |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20110504 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | ALPRAZOLAM |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |