NDC 62856-001

Hexalen

Altretamine

Hexalen is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Eisai Inc.. The primary component is Altretamine.

• Product ID: 62856-001_0a2ea556-16ca-4275-81e0-d721477f047b
• NDC: 62856-001
• Product Type: Human Prescription Drug
• Proprietary Name: Hexalen
• Generic Name: Altretamine
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1990-12-26
• Marketing Category: NDA / NDA
• Application Number: NDA019926
• Labeler Name: Eisai Inc.
• Substance Name: ALTRETAMINE
• Active Ingredient Strength: 50 mg/1
• Pharm Classes: Alkylating Activity [MoA],Alkylating Drug [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 62856-001-10

100 CAPSULE in 1 BOTTLE (62856-001-10)

• Marketing Start Date: 1990-12-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 62856-001-10 [62856000110]

Hexalen CAPSULE

• Marketing Category: NDA
• Application Number: NDA019926
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1990-12-26
• Marketing End Date: 2019-12-31

Drug Details

Active Ingredients

Ingredient	Strength
ALTRETAMINE	50 mg/1

OpenFDA Data

• SPL SET ID: 8456a8db-a7f6-4bc0-86be-e9c8c374140b
• Manufacturer:
  • Eisai Inc.
• UNII:
  • Q8BIH59O7H
• RxNorm Concept Unique ID - RxCUI:
  • 197323
  • 153473
• UPC Code:
  • 0362856001106

Pharmacological Class

• Alkylating Activity [MoA]
• Alkylating Drug [EPC]