NDC 69621-707

TriXylitral

Diclofenac Sodium, Lidocaine Hydrochloride

TriXylitral is a Kit in the Human Prescription Drug category. It is labeled and distributed by Shoreline Pharmaceuticals. The primary component is .

• Product ID: 69621-707_23a932ee-9371-4242-a3be-ac6207141d9f
• NDC: 69621-707
• Product Type: Human Prescription Drug
• Proprietary Name: TriXylitral
• Generic Name: Diclofenac Sodium, Lidocaine Hydrochloride
• Dosage Form: Kit
• Marketing Start Date: 2018-01-15
• Marketing Category: ANDA / ANDA
• Application Number: ANDA202769
• Labeler Name: Shoreline Pharmaceuticals
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 69621-707-00

1 KIT in 1 PACKAGE (69621-707-00) * 1 TUBE in 1 CARTON (59088-371-07) > 85 g in 1 TUBE * 30 in 1 CARTON * 1 BOTTLE in 1 CARTON (59088-372-10) > 150 mL in 1 BOTTLE

• Marketing Start Date: 2018-01-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 69621-707-00 [69621070700]

TriXylitral KIT

• Marketing Category: ANDA
• Application Number: ANDA202769
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2018-01-15
• Marketing End Date: 2019-05-16

Drug Details

OpenFDA Data

• SPL SET ID: 07bbc638-58a4-4568-bf51-4156920308be
• Manufacturer:
  • Shoreline Pharmaceuticals
• RxNorm Concept Unique ID - RxCUI:
  • 857700
  • 1723991
  • 1723996