midazolam hydrochloride

Generic: midazolam hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

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
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

midazolam hydrochloride 1 mg/mL

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-600
Product ID 23155-600_fd88e04f-8d86-401f-8115-2ffdbf2eb54b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090696
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2016-11-08

Pharmacologic Class

Classes
benzodiazepine [epc] benzodiazepines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155600
Hyphenated Format 23155-600

Supplemental Identifiers

RxCUI
1666798
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 ANDA090696 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 CARTON (23155-600-41) / 2 mL in 1 VIAL, SINGLE-DOSE (23155-600-31)
source: ndc

Packages (1)

23155-600-41 25 VIAL, SINGLE-DOSE in 1 CARTON (23155-600-41) / 2 mL in 1 VIAL, SINGLE-DOSE (23155-600-31)

Ingredients (1)

midazolam hydrochloride (1 mg/mL)

Linked Drug Pages (1)

Midazolam hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "fd88e04f-8d86-401f-8115-2ffdbf2eb54b", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798"], "spl_set_id": ["8b690f5c-2923-4c34-a8f7-11af5f546b62"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (23155-600-41)  / 2 mL in 1 VIAL, SINGLE-DOSE (23155-600-31)", "package_ndc": "23155-600-41", "marketing_start_date": "20161108"}], "brand_name": "Midazolam hydrochloride", "product_id": "23155-600_fd88e04f-8d86-401f-8115-2ffdbf2eb54b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "23155-600", "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": "1 mg/mL"}], "application_number": "ANDA090696", "marketing_category": "ANDA", "marketing_start_date": "20161108", "listing_expiration_date": "20261231"}