| NDC Code | 53002-7180-1 |
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| Package Description | 10 CAPSULE in 1 BOTTLE (53002-7180-1) |
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| Product NDC | 53002-7180 |
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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 | RPK Pharmaceuticals, 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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