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NDC 00143-9379-10 Midazolam in Sodium Chloride 1 mg/mL Details
Midazolam in Sodium Chloride 1 mg/mL
Midazolam in Sodium Chloride is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is MIDAZOLAM HYDROCHLORIDE.
MedlinePlus Drug Summary
Midazolam injection is used before medical procedures and surgery to cause drowsiness, relieve anxiety, and prevent any memory of the event. It is also sometimes given as part of the anesthesia during surgery to produce a loss of consciousness. Midazolam injection is also used to cause a state of decreased consciousness in seriously ill people in intensive care units (ICU) who are breathing with the help of a machine. Midazolam injection is in a class of medications called benzodiazepines. It works by slowing activity in the brain to allow relaxation and decreased consciousness.
Related Packages: 00143-9379-10Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Midazolam Injection
Product Information
| NDC | 00143-9379 |
|---|---|
| Product ID | 0143-9379_a6be32fe-dc3d-4ce0-b780-8ba6b4261acc |
| Associated GPIs | |
| GCN Sequence Number | 074967 |
| GCN Sequence Number Description | midazolam HCl in 0.9 % NaCl/PF PLAST. BAG 1 MG/ML INTRAVEN |
| HIC3 | H22 |
| HIC3 Description | GENERAL ANESTHETICS,INJECTABLE-BENZODIAZEPINE TYPE |
| GCN | 39850 |
| HICL Sequence Number | 038614 |
| HICL Sequence Number Description | MIDAZOLAM HCL IN 0.9 % SODIUM CHLORIDE/PF |
| Brand/Generic | Generic |
| Proprietary Name | Midazolam in Sodium Chloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Midazolam in Sodium Chloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/mL |
| Substance Name | MIDAZOLAM HYDROCHLORIDE |
| Labeler Name | Hikma Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Benzodiazepine [EPC], Benzodiazepines [CS] |
| DEA Schedule | CIV |
| Marketing Category | ANDA |
| Application Number | ANDA216159 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00143-9379-10 (00143937910)
| NDC Package Code | 0143-9379-10 |
|---|---|
| Billing NDC | 00143937910 |
| Package | 10 POUCH in 1 CARTON (0143-9379-10) / 1 BAG in 1 POUCH (0143-9379-01) / 50 mL in 1 BAG |
| Marketing Start Date | 2023-05-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |