midazolam
Generic: midazolam hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
midazolam
Generic Name
midazolam hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
midazolam hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-655
Product ID
25021-655_943346c0-d98e-4ac2-a1a2-75427decf2fc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090696
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2012-03-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021655
Hyphenated Format
25021-655
Supplemental Identifiers
RxCUI
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 hydrochloride (source: ndc)
Application Number
ANDA090696 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL in 1 CARTON (25021-655-02) / 2 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "943346c0-d98e-4ac2-a1a2-75427decf2fc", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798"], "spl_set_id": ["e22611dd-1830-40af-9139-7cdb07f5a426"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-655-02) / 2 mL in 1 VIAL", "package_ndc": "25021-655-02", "marketing_start_date": "20120319"}], "brand_name": "midazolam", "product_id": "25021-655_943346c0-d98e-4ac2-a1a2-75427decf2fc", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "25021-655", "dea_schedule": "CIV", "generic_name": "midazolam hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "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_start_date": "20120319", "listing_expiration_date": "20261231"}