midazolam in sodium chloride

Generic: midazolam hydrochloride

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midazolam in sodium chloride
Generic Name midazolam hydrochloride
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

midazolam hydrochloride 1 mg/mL

Manufacturer
Sagent Pharmaceuticals

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
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021688
Hyphenated Format 25021-688

Supplemental Identifiers

RxCUI
2541170 2541171
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 in sodium chloride (source: ndc)
Generic Name midazolam hydrochloride (source: ndc)
Application Number ANDA218993 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
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
source: ndc

Packages (2)

Ingredients (1)

midazolam hydrochloride (1 mg/mL)

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"}