Product NDC: | 17478-524 |
Proprietary Name: | Midazolam |
Non Proprietary Name: | Midazolam Hydrochloride |
Active Ingredient(s): | 5 mg/mL & nbsp; Midazolam Hydrochloride |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-524 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075494 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050506 |
Package NDC: | 17478-524-05 |
Package Description: | 10 VIAL in 1 CARTON (17478-524-05) > 5 mL in 1 VIAL |
NDC Code | 17478-524-05 |
Proprietary Name | Midazolam |
Package Description | 10 VIAL in 1 CARTON (17478-524-05) > 5 mL in 1 VIAL |
Product NDC | 17478-524 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Midazolam Hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20050506 |
Marketing Category Name | ANDA |
Labeler Name | Akorn, Inc. |
Substance Name | MIDAZOLAM HYDROCHLORIDE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |