| NDC Code | 10370-117-00 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (10370-117-00) |
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| Product NDC | 10370-117 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zolpidem Tartrate |
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| Proprietary Name Suffix | Extended-release |
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| Non-Proprietary Name | Zolpidem Tartrate |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20110414 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078148 |
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| Manufacturer | Par Pharmaceutical, Inc. |
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| Substance Name | ZOLPIDEM TARTRATE |
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| Strength | 6.25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | gamma-Aminobutyric Acid-ergic Agonist [EPC],GABA A Agonists [MoA],Pyridines [Chemical/Ingredient],Central Nervous System Depression [PE] |
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| DEA Schedule | CIV |
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