| NDC Code | 0555-0159-04 |
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| Package Description | 500 CAPSULE in 1 BOTTLE (0555-0159-04) |
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| Product NDC | 0555-0159 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Chlordiazepoxide Hydrochloride |
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| Non-Proprietary Name | Chlordiazepoxide Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 19760701 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA084769 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | CHLORDIAZEPOXIDE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Benzodiazepine [EPC], Benzodiazepines [CS] |
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| DEA Schedule | CIV |
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