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 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-288
Product ID
63323-288_75465ceb-e894-487d-aa80-671fa0841fce
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
63323288
Hyphenated Format
63323-288
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
naropin (source: ndc)
Generic Name
ropivacaine hydrochloride (source: ndc)
Application Number
NDA020533 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 5 AMPULE in 1 BOX (63323-288-27) / 20 mL in 1 AMPULE (63323-288-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (3)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL"], "spl_id": "75465ceb-e894-487d-aa80-671fa0841fce", "openfda": {"unii": ["V910P86109"], "rxcui": ["1734084", "1734086", "1734090", "1734091"], "spl_set_id": ["56dfabf7-f7a8-4601-b17a-cb16fb995b0f"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 AMPULE in 1 BOX (63323-288-27) / 20 mL in 1 AMPULE (63323-288-25)", "package_ndc": "63323-288-27", "marketing_start_date": "20090804"}], "brand_name": "Naropin", "product_id": "63323-288_75465ceb-e894-487d-aa80-671fa0841fce", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Local Anesthesia [PE]"], "product_ndc": "63323-288", "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": "10 mg/mL"}], "application_number": "NDA020533", "marketing_category": "NDA", "marketing_start_date": "19960924", "listing_expiration_date": "20261231"}