dexlido-m kit

Generic: dexamethasone sodium phosphate, lidocaine hydrochloride, maricaine, povidine iodine

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

Drug Facts

Product Profile

Brand Name dexlido-m kit
Generic Name dexamethasone sodium phosphate, lidocaine hydrochloride, maricaine, povidine iodine
Labeler asclemed usa, inc.
Dosage Form KIT
Routes
EPIDURAL INFILTRATION INTRAMUSCULAR INTRAVENOUS TOPICAL
Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-769
Product ID 76420-769_47db0814-8bb0-9752-e063-6294a90a51d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2027-12-31
Marketing Start 2014-07-25

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420769
Hyphenated Format 76420-769

Supplemental Identifiers

RxCUI
797544 797730 1725078 1737568 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 dexlido-m kit (source: ndc)
Generic Name dexamethasone sodium phosphate, lidocaine hydrochloride, maricaine, povidine iodine (source: ndc)
Routes
EPIDURAL INFILTRATION INTRAMUSCULAR INTRAVENOUS TOPICAL
source: ndc

Resolved Composition

Strengths
  • 0.25 %
  • 25 mg/10 ml
  • 2.5 mg/ml
  • 75 mg/30 ml
  • 125 mg/50 ml
  • 0.5 %
  • 50 mg/10 ml
  • 5 mg/ml
  • 150 mg/30 ml
  • 250 mg/50 ml
  • 0.75 %
  • 75 mg/10 ml
  • 7.5 mg/ml
  • 225 mg/30 ml
  • 10 mg
  • 10 mg/ml
  • 1 ml
  • 1 %
  • 2 ml
  • 10 %
  • 9.85 %
  • 70 %
source: label
Packaging
  • 1 KIT in 1 CARTON (76420-769-01) * 10 mL in 1 VIAL, SINGLE-DOSE (0409-1159-18) * .9 mL in 1 PACKET (67777-419-02) * 5 mL in 1 POUCH * 10 AMPULE in 1 CARTON (55150-158-72) / 2 mL in 1 AMPULE * 25 VIAL in 1 TRAY (63323-506-01) / 1 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INFILTRATION", "INTRAMUSCULAR", "INTRAVENOUS", "TOPICAL"], "spl_id": "47db0814-8bb0-9752-e063-6294a90a51d1", "openfda": {"rxcui": ["797544", "797730", "1725078", "1737568", "1812079"], "spl_set_id": ["d3fd1d51-7749-4e1e-a8b5-8a151392f66d"], "manufacturer_name": ["Asclemed USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (76420-769-01)  *  10 mL in 1 VIAL, SINGLE-DOSE (0409-1159-18)  *  .9 mL in 1 PACKET (67777-419-02)  *  5 mL in 1 POUCH *  10 AMPULE in 1 CARTON (55150-158-72)  / 2 mL in 1 AMPULE *  25 VIAL in 1 TRAY (63323-506-01)  / 1 mL in 1 VIAL", "package_ndc": "76420-769-01", "marketing_start_date": "20160523"}], "brand_name": "Dexlido-M Kit", "product_id": "76420-769_47db0814-8bb0-9752-e063-6294a90a51d1", "dosage_form": "KIT", "product_ndc": "76420-769", "generic_name": "Dexamethasone Sodium Phosphate, Lidocaine Hydrochloride, maricaine, Povidine Iodine", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexlido-M Kit", "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20140725", "listing_expiration_date": "20271231"}