midazolam

Generic: midazolam

Labeler: almaject, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midazolam
Generic Name midazolam
Labeler almaject, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

midazolam hydrochloride 1 mg/mL

Manufacturer
Almaject, Inc.

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
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72611741
Hyphenated Format 72611-741

Supplemental Identifiers

RxCUI
1666798
UPC
0372611741253
UNII
W7TTW573JJ

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (72611-741-25) / 2 mL in 1 VIAL, SINGLE-DOSE (72611-741-01)
source: ndc

Packages (1)

Ingredients (1)

midazolam hydrochloride (1 mg/mL)

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"}