midazolam hydrochloride
Generic: midazolam hydrochloride
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
midazolam hydrochloride
Generic Name
midazolam hydrochloride
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
midazolam hydrochloride 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
23155-601
Product ID
23155-601_e20feff9-3aca-4bc1-a5c3-44fff8a9459c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090850
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2016-11-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155601
Hyphenated Format
23155-601
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 hydrochloride (source: ndc)
Generic Name
midazolam hydrochloride (source: ndc)
Application Number
ANDA090850 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 10 VIAL, MULTI-DOSE in 1 CARTON (23155-601-41) / 5 mL in 1 VIAL, MULTI-DOSE (23155-601-31)
- 10 VIAL, MULTI-DOSE in 1 CARTON (23155-601-42) / 10 mL in 1 VIAL, MULTI-DOSE (23155-601-32)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "e20feff9-3aca-4bc1-a5c3-44fff8a9459c", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["311702"], "spl_set_id": ["843cc25e-45ea-4372-ae34-843f805fa869"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (23155-601-41) / 5 mL in 1 VIAL, MULTI-DOSE (23155-601-31)", "package_ndc": "23155-601-41", "marketing_start_date": "20161107"}, {"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (23155-601-42) / 10 mL in 1 VIAL, MULTI-DOSE (23155-601-32)", "package_ndc": "23155-601-42", "marketing_start_date": "20161107"}], "brand_name": "Midazolam hydrochloride", "product_id": "23155-601_e20feff9-3aca-4bc1-a5c3-44fff8a9459c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "23155-601", "dea_schedule": "CIV", "generic_name": "Midazolam hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "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": "20161107", "listing_expiration_date": "20261231"}