ropidex

Generic: dexamethasone sodium phosphate, ropivacaine hydrochloride, povidine iodine

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name ropidex
Generic Name dexamethasone sodium phosphate, ropivacaine hydrochloride, povidine iodine
Labeler asclemed usa, inc.
Dosage Form KIT
Routes
EPIDURAL INFILTRATION INTRAMUSCULAR INTRAVENOUS PERINEURAL TOPICAL
Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-219
Product ID 76420-219_23b36bd4-0dbc-366a-e063-6294a90a1565
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2019-06-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420219
Hyphenated Format 76420-219

Supplemental Identifiers

RxCUI
797730 1734483 1812079

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 ropidex (source: ndc)
Generic Name dexamethasone sodium phosphate, ropivacaine hydrochloride, povidine iodine (source: ndc)
Routes
EPIDURAL INFILTRATION INTRAMUSCULAR INTRAVENOUS PERINEURAL TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg
  • 10 mg/ml
  • 1 ml
  • 0.5 %
  • 100 mg/20 ml
  • 5 mg/ml
  • 20 ml
  • 10 %
  • 9.85 %
source: label
Packaging
  • 1 KIT in 1 CARTON (76420-219-01) * 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-197-20) / 20 mL in 1 VIAL, SINGLE-DOSE * .9 mL in 1 PACKET (67777-419-02) * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIAL
source: ndc

Packages (1)

76420-219-01 1 KIT in 1 CARTON (76420-219-01) * 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-197-20) / 20 mL in 1 VIAL, SINGLE-DOSE * .9 mL in 1 PACKET (67777-419-02) * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIAL

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Ropidex ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EPIDURAL", "INFILTRATION", "INTRAMUSCULAR", "INTRAVENOUS", "PERINEURAL", "TOPICAL"], "spl_id": "23b36bd4-0dbc-366a-e063-6294a90a1565", "openfda": {"rxcui": ["797730", "1734483", "1812079"], "spl_set_id": ["2577c1ba-8aff-4098-ba11-a375e9ce3caa"], "manufacturer_name": ["Asclemed USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (76420-219-01)  *  25 VIAL, SINGLE-DOSE in 1 CARTON (55150-197-20)  / 20 mL in 1 VIAL, SINGLE-DOSE *  .9 mL in 1 PACKET (67777-419-02)  *  25 VIAL in 1 TRAY (63323-506-01)  / 1 mL in 1 VIAL", "package_ndc": "76420-219-01", "marketing_start_date": "20190610"}], "brand_name": "Ropidex", "product_id": "76420-219_23b36bd4-0dbc-366a-e063-6294a90a1565", "dosage_form": "KIT", "product_ndc": "76420-219", "generic_name": "Dexamethasone Sodium Phosphate, Ropivacaine Hydrochloride, Povidine Iodine", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ropidex", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20190610", "listing_expiration_date": "20261231"}