ropivacaine hydrochloride
Generic: ropivacaine hydrochloride
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ropivacaine hydrochloride
Generic Name
ropivacaine hydrochloride
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
ropivacaine hydrochloride 7.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9265
Product ID
0143-9265_ca74bdef-8c1f-4919-a7e9-a7655953b3af
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214074
Listing Expiration
2027-12-31
Marketing Start
2025-11-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439265
Hyphenated Format
0143-9265
Supplemental Identifiers
RxCUI
UPC
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
ropivacaine hydrochloride (source: ndc)
Generic Name
ropivacaine hydrochloride (source: ndc)
Application Number
ANDA214074 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7.5 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9265-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0143-9265-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL"], "spl_id": "ca74bdef-8c1f-4919-a7e9-a7655953b3af", "openfda": {"upc": ["0301439265108", "0301439266105", "0301439263104", "0301439264101"], "unii": ["V910P86109"], "rxcui": ["905189", "1734084", "1734207", "1734475"], "spl_set_id": ["35743510-728d-407b-b501-cf019665cd35"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9265-10) / 20 mL in 1 VIAL, SINGLE-DOSE (0143-9265-01)", "package_ndc": "0143-9265-10", "marketing_start_date": "20251118"}], "brand_name": "Ropivacaine Hydrochloride", "product_id": "0143-9265_ca74bdef-8c1f-4919-a7e9-a7655953b3af", "dosage_form": "INJECTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "0143-9265", "generic_name": "Ropivacaine Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropivacaine Hydrochloride", "active_ingredients": [{"name": "ROPIVACAINE HYDROCHLORIDE", "strength": "7.5 mg/mL"}], "application_number": "ANDA214074", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20271231"}