NDC 59088-716

Diclotrex

Diclofenac Sodium, Camphor, Menthol

Diclotrex is a Kit in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is .

• Product ID: 59088-716_4cf67e3a-fbb8-4284-95c0-f87fa220a7dc
• NDC: 59088-716
• Product Type: Human Prescription Drug
• Proprietary Name: Diclotrex
• Generic Name: Diclofenac Sodium, Camphor, Menthol
• Dosage Form: Kit
• Marketing Start Date: 2018-10-23
• Marketing Category: ANDA / ANDA
• Application Number: ANDA202769
• Labeler Name: PureTek Corporation
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 59088-716-00

1 KIT in 1 KIT (59088-716-00) * 1 CARTON in 1 KIT > 1 BOTTLE in 1 CARTON (59088-372-10) > 150 mL in 1 BOTTLE * 85 g in 1 BOTTLE, WITH APPLICATOR (59088-283-07)

• Marketing Start Date: 2018-10-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59088-716-00 [59088071600]

Diclotrex KIT

• Marketing Category: ANDA
• Application Number: ANDA202769
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-10-23

Drug Details

OpenFDA Data

• SPL SET ID: 513e06f5-9bb4-485b-bcc4-923c0ff17fbc
• Manufacturer:
  • PureTek Corporation
• RxNorm Concept Unique ID - RxCUI:
  • 857700
  • 1039731

NDC Crossover Matching brand name "Diclotrex" or generic name "Diclofenac Sodium, Camphor, Menthol"

NDC	Brand Name	Generic Name
59088-716	Diclotrex	diclofenac sodium, camphor, menthol
59088-785	Diclotrex	diclofenac sodium, camphor, menthol