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Flurazepam Hydrochloride
Flurazepam Hydrochloride - 55289-038-30 - (flurazepam hydrochloride)
Drug Information of Flurazepam Hydrochloride
| Product NDC: | 55289-038 |
| Proprietary Name: | Flurazepam Hydrochloride |
| Non Proprietary Name: | flurazepam hydrochloride |
| Active Ingredient(s): | 30 mg/1 & nbsp; flurazepam hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flurazepam Hydrochloride
| Product NDC: | 55289-038 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070345 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100716 |
Package Information of Flurazepam Hydrochloride
| Package NDC: | 55289-038-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-038-30) |
NDC Information of Flurazepam Hydrochloride
| NDC Code | 55289-038-30 |
| Proprietary Name | Flurazepam Hydrochloride |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-038-30) |
| Product NDC | 55289-038 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | flurazepam hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100716 |
| Marketing Category Name | ANDA |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | FLURAZEPAM HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
