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Ambien
Ambien - 0024-5421-50 - (zolpidem tartrate)
Drug Information of Ambien
| Product NDC: | 0024-5421 |
| Proprietary Name: | Ambien |
| Non Proprietary Name: | zolpidem tartrate |
| Active Ingredient(s): | 10 mg/1 & nbsp; zolpidem tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ambien
| Product NDC: | 0024-5421 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019908 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930401 |
Package Information of Ambien
| Package NDC: | 0024-5421-50 |
| Package Description: | 500 TABLET, FILM COATED in 1 BOTTLE (0024-5421-50) |
NDC Information of Ambien
| NDC Code | 0024-5421-50 |
| Proprietary Name | Ambien |
| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0024-5421-50) |
| Product NDC | 0024-5421 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | zolpidem tartrate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19930401 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | ZOLPIDEM TARTRATE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [Chemical/Ingredient],Central Nervous System Depression [PE] |
