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Flurazepam
Flurazepam - 21695-363-30 - (Flurazepam Hydrochloride)
Drug Information of Flurazepam
| Product NDC: | 21695-363 |
| Proprietary Name: | Flurazepam |
| 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
| Product NDC: | 21695-363 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071108 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19861208 |
Package Information of Flurazepam
| Package NDC: | 21695-363-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-363-30) |
NDC Information of Flurazepam
| NDC Code | 21695-363-30 |
| Proprietary Name | Flurazepam |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-363-30) |
| Product NDC | 21695-363 |
| 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 | Rebel Distributors Corp |
| Substance Name | FLURAZEPAM HYDROCHLORIDE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
