| NDC Code: |
0228-3481 |
| Proprietary Name: |
Zolpidem Tartrate |
| Suffix: |
|
| Non-Proprietary Name: |
Zolpidem Tartrate |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
13-10-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078179 |
| Labeler: |
ACTAVIS ELIZABETH LLC |
| Substance Name: |
ZOLPIDEM TARTRATE |
| Active Numerator Strength: |
6.25 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [Chemical/Ingredient],Central Nervous System Depression [PE] |
| DEA Schedule: |
CIV |
