Product NDC: | 52959-236 |
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) |
Product NDC: | 52959-236 |
Labeler Name: | H.J. Harkins Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071108 |
Marketing Category: | ANDA |
Start Marketing Date: | 19861208 |
Package NDC: | 52959-236-30 |
Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (52959-236-30) |
NDC Code | 52959-236-30 |
Proprietary Name | Flurazepam |
Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (52959-236-30) |
Product NDC | 52959-236 |
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 | H.J. Harkins Company, Inc. |
Substance Name | FLURAZEPAM HYDROCHLORIDE |
Strength Number | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |