| NDC Code | 47335-307-13 |
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| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-307-13) |
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| Product NDC | 47335-307 |
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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 | 20170515 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204170 |
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| Manufacturer | Sun Pharmaceutical Industries, 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 | Central Nervous System Depression [PE], GABA A Agonists [MoA], Pyridines [CS], gamma-Aminobutyric Acid-ergic Agonist [EPC] |
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| DEA Schedule | CIV |
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