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Flurazepam
Flurazepam - 0143-3367-01 - (Flurazepam Hydrochloride)
Drug Information of Flurazepam
| Product NDC: | 0143-3367 |
| Proprietary Name: | Flurazepam |
| Non Proprietary Name: | Flurazepam Hydrochloride |
| Active Ingredient(s): | 15 mg/1 & nbsp; Flurazepam Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Flurazepam
| Product NDC: | 0143-3367 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077107 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19861208 |
Package Information of Flurazepam
| Package NDC: | 0143-3367-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (0143-3367-01) |
NDC Information of Flurazepam
| NDC Code | 0143-3367-01 |
| Proprietary Name | Flurazepam |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (0143-3367-01) |
| Product NDC | 0143-3367 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Flurazepam Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19861208 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | FLURAZEPAM HYDROCHLORIDE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
