NDC Code |
66336-460-20 |
Proprietary Name |
Zolpidem Tartrate |
Package Description |
20 TABLET, FILM COATED in 1 BOTTLE (66336-460-20) |
Product NDC |
66336-460 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
zolpidem tartrate |
Dosage Form Name |
TABLET, FILM COATED |
Route Name |
ORAL |
Start Marketing Date |
20081121 |
Marketing Category Name |
ANDA |
Labeler Name |
Dispensing Solutions, Inc. |
Substance Name |
ZOLPIDEM TARTRATE |
Strength Number |
5 |
Strength Unit |
mg/1 |
Pharmaceutical Classes |
gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [Chemical/Ingredient],Central Nervous System Depression [PE] |