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Chlordiazepoxide Hydrochloride
Chlordiazepoxide Hydrochloride - 42291-212-90 - (Chlordiazepoxide Hydrochloride)
Drug Information of Chlordiazepoxide Hydrochloride
| Product NDC: | 42291-212 |
| Proprietary Name: | Chlordiazepoxide Hydrochloride |
| Non Proprietary Name: | Chlordiazepoxide Hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; Chlordiazepoxide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, GELATIN COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chlordiazepoxide Hydrochloride
| Product NDC: | 42291-212 |
| Labeler Name: | AvKARE, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085475 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020926 |
Package Information of Chlordiazepoxide Hydrochloride
| Package NDC: | 42291-212-90 |
| Package Description: | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (42291-212-90) |
NDC Information of Chlordiazepoxide Hydrochloride
| NDC Code | 42291-212-90 |
| Proprietary Name | Chlordiazepoxide Hydrochloride |
| Package Description | 90 CAPSULE, GELATIN COATED in 1 BOTTLE (42291-212-90) |
| Product NDC | 42291-212 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlordiazepoxide Hydrochloride |
| Dosage Form Name | CAPSULE, GELATIN COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020926 |
| Marketing Category Name | ANDA |
| Labeler Name | AvKARE, Inc. |
| Substance Name | CHLORDIAZEPOXIDE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
