Home
>
National Drug Code (NDC)
>
Midazolam Hydrochloride
Midazolam Hydrochloride - 55390-137-02 - (Midazolam Hydrochloride)
Drug Information of Midazolam Hydrochloride
| Product NDC: | 55390-137 |
| Proprietary Name: | Midazolam Hydrochloride |
| Non Proprietary Name: | Midazolam Hydrochloride |
| Active Ingredient(s): | 1 mg/mL & nbsp; Midazolam Hydrochloride |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Midazolam Hydrochloride
| Product NDC: | 55390-137 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075421 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000621 |
Package Information of Midazolam Hydrochloride
| Package NDC: | 55390-137-02 |
| Package Description: | 10 VIAL in 1 BOX (55390-137-02) > 2 mL in 1 VIAL |
NDC Information of Midazolam Hydrochloride
| NDC Code | 55390-137-02 |
| Proprietary Name | Midazolam Hydrochloride |
| Package Description | 10 VIAL in 1 BOX (55390-137-02) > 2 mL in 1 VIAL |
| Product NDC | 55390-137 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Midazolam Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20000621 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
