Midazolam HCl is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Cantrell Drug Company. The primary component is Midazolam Hydrochloride.
| Product ID | 52533-001_2a80c18a-119b-4df9-a9d2-b9bf8038d900 |
| NDC | 52533-001 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Midazolam HCl |
| Generic Name | Midazolam Hcl |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2011-12-05 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Cantrell Drug Company |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Active Ingredient Strength | 1 mg/mL |
| Pharm Classes | Benzodiazepine [EPC],Benzodiazepines [CS] |
| DEA Schedule | CIV |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2011-12-05 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-08-02 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-08-02 |
| Marketing End Date | 2015-01-14 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2012-04-13 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-12-05 |
| Marketing End Date | 2014-01-14 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-04-30 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2012-04-13 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2011-12-05 |
| Inactivation Date | 2019-11-27 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-06-28 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-04-25 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-04-08 |
| Inactivation Date | 2020-01-31 |
| Marketing Category | unapproved drug other |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2013-11-01 |
| Inactivation Date | 2019-11-27 |
| Ingredient | Strength |
|---|---|
| MIDAZOLAM HYDROCHLORIDE | 1 mg/mL |
| SPL SET ID: | d9cd30df-4888-4041-8416-b59ecd89a063 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 52533-001 | Midazolam HCl | Midazolam HCl |
| 52533-157 | Midazolam HCl | Midazolam HCl |