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Midazolam Hydrochloride
Midazolam Hydrochloride - 0409-2308-50 - (MIDAZOLAM HYDROCHLORIDE)
Drug Information of Midazolam Hydrochloride
| Product NDC: | 0409-2308 |
| Proprietary Name: | Midazolam Hydrochloride |
| Non Proprietary Name: | MIDAZOLAM HYDROCHLORIDE |
| Active Ingredient(s): | 5 mg/mL & nbsp; MIDAZOLAM HYDROCHLORIDE |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Midazolam Hydrochloride
| Product NDC: | 0409-2308 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075857 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020722 |
Package Information of Midazolam Hydrochloride
| Package NDC: | 0409-2308-50 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-2308-50) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Midazolam Hydrochloride
| NDC Code | 0409-2308-50 |
| Proprietary Name | Midazolam Hydrochloride |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-2308-50) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-2308 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MIDAZOLAM HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20020722 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
