midazolam
Generic: midazolam
Labeler: almaject, inc.Drug Facts
Product Profile
Brand Name
midazolam
Generic Name
midazolam
Labeler
almaject, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
midazolam hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72611-741
Product ID
72611-741_53563167-5000-bd14-bfa9-a805bc8c200f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090696
DEA Schedule
civ
Marketing Start
2020-04-14
Marketing End
2026-04-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72611741
Hyphenated Format
72611-741
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
midazolam (source: ndc)
Generic Name
midazolam (source: ndc)
Application Number
ANDA090696 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (72611-741-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72611-741-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "53563167-5000-bd14-bfa9-a805bc8c200f", "openfda": {"upc": ["0372611741253"], "unii": ["W7TTW573JJ"], "rxcui": ["1666798"], "spl_set_id": ["c33919da-1d84-ed01-a5e5-62330407336e"], "manufacturer_name": ["Almaject, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (72611-741-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72611-741-01)", "package_ndc": "72611-741-25", "marketing_end_date": "20260401", "marketing_start_date": "20200414"}], "brand_name": "midazolam", "product_id": "72611-741_53563167-5000-bd14-bfa9-a805bc8c200f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72611-741", "dea_schedule": "CIV", "generic_name": "midazolam", "labeler_name": "Almaject, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA090696", "marketing_category": "ANDA", "marketing_end_date": "20260401", "marketing_start_date": "20200414"}