midazolam in sodium chloride
Generic: midazolam hydrochloride
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
midazolam in sodium chloride
Generic Name
midazolam hydrochloride
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
midazolam hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-688
Product ID
25021-688_44922f28-68c0-45c6-ad4c-0cc7706a78b4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218993
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2025-04-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021688
Hyphenated Format
25021-688
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 in sodium chloride (source: ndc)
Generic Name
midazolam hydrochloride (source: ndc)
Application Number
ANDA218993 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 BAG in 1 CARTON (25021-688-82) / 50 mL in 1 BAG
- 20 BAG in 1 CARTON (25021-688-87) / 100 mL in 1 BAG
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "44922f28-68c0-45c6-ad4c-0cc7706a78b4", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["2541170", "2541171"], "spl_set_id": ["c546cfd4-4f2b-4b94-aa47-995595f1a146"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BAG in 1 CARTON (25021-688-82) / 50 mL in 1 BAG", "package_ndc": "25021-688-82", "marketing_start_date": "20250415"}, {"sample": false, "description": "20 BAG in 1 CARTON (25021-688-87) / 100 mL in 1 BAG", "package_ndc": "25021-688-87", "marketing_start_date": "20250415"}], "brand_name": "Midazolam in Sodium Chloride", "product_id": "25021-688_44922f28-68c0-45c6-ad4c-0cc7706a78b4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "25021-688", "dea_schedule": "CIV", "generic_name": "Midazolam Hydrochloride", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam in Sodium Chloride", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA218993", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}