NDC 62856-601

Panretin

Alitretinoin

Panretin is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Eisai Inc.. The primary component is Alitretinoin.

• Product ID: 62856-601_50ab2ed7-651c-4952-91d6-5011709ae429
• NDC: 62856-601
• Product Type: Human Prescription Drug
• Proprietary Name: Panretin
• Generic Name: Alitretinoin
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2009-02-03
• Marketing Category: NDA / NDA
• Application Number: NDA020886
• Labeler Name: Eisai Inc.
• Substance Name: ALITRETINOIN
• Active Ingredient Strength: 60 mg/60g
• Pharm Classes: Retinoid [EPC],Retinoids [CS]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 62856-601-22

60 g in 1 TUBE (62856-601-22)

• Marketing Start Date: 2009-02-03
• Marketing End Date: 2021-10-31
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62856-601-22 [62856060122]

Panretin GEL

• Marketing Category: NDA
• Application Number: NDA020886
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2009-02-03
• Marketing End Date: 2021-10-31

Drug Details

Active Ingredients

Ingredient	Strength
ALITRETINOIN	60 mg/60g

OpenFDA Data

• SPL SET ID: 13c5de6d-d266-4d83-99c4-072ef104e7ff
• Manufacturer:
  • Eisai Inc.
• UNII:
  • 1UA8E65KDZ
• RxNorm Concept Unique ID - RxCUI:
  • 213502
  • 313847

Pharmacological Class

• Retinoid [EPC]
• Retinoids [CS]

NDC Crossover Matching brand name "Panretin" or generic name "Alitretinoin"

NDC	Brand Name	Generic Name
59212-601	PANRETIN	alitretinoin
62856-601	Panretin	Alitretinoin