Product NDC: | 0409-3213 |
Proprietary Name: | Diazepam |
Non Proprietary Name: | DIAZEPAM |
Active Ingredient(s): | 5 mg/mL & nbsp; DIAZEPAM |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0409-3213 |
Labeler Name: | Hospira, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA071583 |
Marketing Category: | ANDA |
Start Marketing Date: | 19871013 |
Package NDC: | 0409-3213-02 |
Package Description: | 5 VIAL, MULTI-DOSE in 1 CARTON (0409-3213-02) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 0409-3213-02 |
Proprietary Name | Diazepam |
Package Description | 5 VIAL, MULTI-DOSE in 1 CARTON (0409-3213-02) > 10 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 0409-3213 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DIAZEPAM |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 19871013 |
Marketing Category Name | ANDA |
Labeler Name | Hospira, Inc. |
Substance Name | DIAZEPAM |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |