naropin
Generic: ropivacaine hydrochloride
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
naropin
Generic Name
ropivacaine hydrochloride
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
ropivacaine hydrochloride 7.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-287
Product ID
63323-287_cdcd6c58-85cf-4d7e-9d97-b7c282a4f6b9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA020533
Listing Expiration
2026-12-31
Marketing Start
1996-09-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323287
Hyphenated Format
63323-287
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
naropin (source: ndc)
Generic Name
ropivacaine hydrochloride (source: ndc)
Application Number
NDA020533 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 7.5 mg/mL
Packaging
- 5 AMPULE in 1 BOX (63323-287-20) / 20 mL in 1 AMPULE (63323-287-01)
- 25 VIAL, SINGLE-DOSE in 1 CARTON (63323-287-21) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-287-03)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "PERINEURAL"], "spl_id": "cdcd6c58-85cf-4d7e-9d97-b7c282a4f6b9", "openfda": {"upc": ["0363323286033", "0363323285074", "0363323285036", "0363323285579", "0363323287030", "0363323286095", "0363323288075", "0363323286330", "0363323286057", "0363323288037", "0363323286118", "0363323285517"], "unii": ["V910P86109"], "rxcui": ["905189", "905191", "1734084", "1734086", "1734090", "1734091", "1734203", "1734204", "1734207", "1734208", "1734347", "1734348", "1734355", "1734356", "1734475", "1734476", "1734479", "1734480", "1734481", "1734482", "1734483", "1734484"], "spl_set_id": ["23d2d448-a744-4877-9f2d-7e57c198da89"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 AMPULE in 1 BOX (63323-287-20) / 20 mL in 1 AMPULE (63323-287-01)", "package_ndc": "63323-287-20", "marketing_start_date": "20110531"}, {"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (63323-287-21) / 20 mL in 1 VIAL, SINGLE-DOSE (63323-287-03)", "package_ndc": "63323-287-21", "marketing_start_date": "20110531"}], "brand_name": "Naropin", "product_id": "63323-287_cdcd6c58-85cf-4d7e-9d97-b7c282a4f6b9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "63323-287", "generic_name": "ROPIVACAINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naropin", "active_ingredients": [{"name": "ROPIVACAINE HYDROCHLORIDE", "strength": "7.5 mg/mL"}], "application_number": "NDA020533", "marketing_category": "NDA", "marketing_start_date": "19960924", "listing_expiration_date": "20261231"}