| NDC Code | 68084-889-21 |
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| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-889-21) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-889-11) |
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| Product NDC | 68084-889 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zolpidem Tartrate |
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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 | 20160413 |
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| End Marketing Date | 20180630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078179 |
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| Manufacturer | American Health Packaging |
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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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