midazolam
Generic: midazolam
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
midazolam
Generic Name
midazolam
Labeler
civica, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
midazolam hydrochloride 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72572-430
Product ID
72572-430_1b0844b9-17fb-4f81-b438-6fcbb850a0a7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075243
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2019-12-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572430
Hyphenated Format
72572-430
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 (source: ndc)
Generic Name
midazolam (source: ndc)
Application Number
ANDA075243 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 25 VIAL in 1 CARTON (72572-430-25) / 2 mL in 1 VIAL (72572-430-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "1b0844b9-17fb-4f81-b438-6fcbb850a0a7", "openfda": {"unii": ["W7TTW573JJ"], "rxcui": ["1666798", "1666800"], "spl_set_id": ["f0c8b6cd-9efc-4344-9212-fbdd3b8e2f9b"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-430-25) / 2 mL in 1 VIAL (72572-430-01)", "package_ndc": "72572-430-25", "marketing_start_date": "20191210"}], "brand_name": "Midazolam", "product_id": "72572-430_1b0844b9-17fb-4f81-b438-6fcbb850a0a7", "dosage_form": "INJECTION", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "72572-430", "dea_schedule": "CIV", "generic_name": "Midazolam", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Midazolam", "active_ingredients": [{"name": "MIDAZOLAM HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA075243", "marketing_category": "ANDA", "marketing_start_date": "20191210", "listing_expiration_date": "20261231"}