NDC 76420-767

Dexlido Kit

Dexamethasone Sodium Phosphate, Lidocaine Hydrochloride, Povidine Iodine

Dexlido Kit is a Infiltration; Intramuscular; Intravenous; Topical Kit in the Human Prescription Drug category. It is labeled and distributed by Asclemed Usa, Inc.. The primary component is .

• Product ID: 76420-767_7acc6424-2348-6370-e053-2a91aa0a5917
• NDC: 76420-767
• Product Type: Human Prescription Drug
• Proprietary Name: Dexlido Kit
• Generic Name: Dexamethasone Sodium Phosphate, Lidocaine Hydrochloride, Povidine Iodine
• Dosage Form: Kit
• Route of Administration: INFILTRATION; INTRAMUSCULAR; INTRAVENOUS; TOPICAL
• Marketing Start Date: 2014-07-25
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Asclemed USA, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 76420-767-01

1 KIT in 1 CARTON (76420-767-01) * 2 mL in 1 AMPULE (0409-4713-42) * .9 mL in 1 PACKET (67777-419-02) * 5 mL in 1 POUCH * 25 VIAL in 1 TRAY (63323-506-01) > 1 mL in 1 VIAL

• Marketing Start Date: 2016-05-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 76420-767-01 [76420076701]

Dexlido Kit KIT

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-05-23

Drug Details

OpenFDA Data

• SPL SET ID: 65428186-5fbb-4e1a-ae60-8824f3d62179
• Manufacturer:
  • Asclemed USA, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 1812079
  • 797544
  • 1737568
  • 797730