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Zolpidem Tartrate
Zolpidem Tartrate - 51079-724-20 - (zolpidem tartrate)
Drug Information of Zolpidem Tartrate
| Product NDC: | 51079-724 |
| Proprietary Name: | Zolpidem Tartrate |
| Non Proprietary Name: | zolpidem tartrate |
| Active Ingredient(s): | 5 mg/1 & nbsp; zolpidem tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zolpidem Tartrate
| Product NDC: | 51079-724 |
| Labeler Name: | Mylan Institutional Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076578 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120109 |
Package Information of Zolpidem Tartrate
| Package NDC: | 51079-724-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-724-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-724-01) |
NDC Information of Zolpidem Tartrate
| NDC Code | 51079-724-20 |
| Proprietary Name | Zolpidem Tartrate |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-724-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-724-01) |
| Product NDC | 51079-724 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | zolpidem tartrate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120109 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Institutional 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] |
