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CHLORDIAZE-POXIDE HCL
CHLORDIAZE-POXIDE HCL - 55289-061-60 - (chlordiazepoxide hydrochloride)
Drug Information of CHLORDIAZE-POXIDE HCL
| Product NDC: | 55289-061 |
| Proprietary Name: | CHLORDIAZE-POXIDE HCL |
| Non Proprietary Name: | chlordiazepoxide hydrochloride |
| Active Ingredient(s): | 10 mg/1 & nbsp; chlordiazepoxide hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CHLORDIAZE-POXIDE HCL
| Product NDC: | 55289-061 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040746 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100101 |
Package Information of CHLORDIAZE-POXIDE HCL
| Package NDC: | 55289-061-60 |
| Package Description: | 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-061-60) |
NDC Information of CHLORDIAZE-POXIDE HCL
| NDC Code | 55289-061-60 |
| Proprietary Name | CHLORDIAZE-POXIDE HCL |
| Package Description | 60 CAPSULE in 1 BOTTLE, PLASTIC (55289-061-60) |
| Product NDC | 55289-061 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | chlordiazepoxide hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | CHLORDIAZEPOXIDE HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
