midazolam hydrochloride

Generic: midazolam hydrochloride

Labeler: jvet pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name midazolam hydrochloride
Generic Name midazolam hydrochloride
Labeler jvet pharmaceuticals llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

midazolam hydrochloride 5 mg/mL

Manufacturer
Jvet Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 86211-111
Product ID 86211-111_ad8a2323-085c-41eb-bbbd-718c9ea50f9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090850
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-10-21

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 86211111
Hyphenated Format 86211-111

Supplemental Identifiers

RxCUI
311702
UPC
0386211111101
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 hydrochloride (source: ndc)
Generic Name midazolam hydrochloride (source: ndc)
Application Number ANDA090850 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 10 VIAL, MULTI-DOSE in 1 CARTON (86211-111-10) / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

Ingredients (1)

midazolam hydrochloride (5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ad8a2323-085c-41eb-bbbd-718c9ea50f9f", "openfda": {"upc": ["0386211111101"], "unii": ["W7TTW573JJ"], "rxcui": ["311702"], "spl_set_id": ["a84ddd02-1f5f-4311-9dae-2a5cb4064bf3"], "manufacturer_name": ["Jvet Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (86211-111-10)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "86211-111-10", "marketing_start_date": "20251021"}], "brand_name": "Midazolam Hydrochloride", "product_id": "86211-111_ad8a2323-085c-41eb-bbbd-718c9ea50f9f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "86211-111", "dea_schedule": "CIV", "generic_name": "Midazolam Hydrochloride", "labeler_name": "Jvet Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam Hydrochloride", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA090850", "marketing_category": "ANDA", "marketing_start_date": "20251021", "listing_expiration_date": "20261231"}