NDC 72536-0920

Indium In 111 Oxyquinoline

Indium In-111 Oxyquinoline

Indium In 111 Oxyquinoline is a Intravenous Liquid in the Human Prescription Drug category. It is labeled and distributed by Bwxt Itg Canada, Inc.. The primary component is Indium In-111 Oxyquinoline.

• Product ID: 72536-0920_0fdde55c-0f72-4e56-a727-10917c278f83
• NDC: 72536-0920
• Product Type: Human Prescription Drug
• Proprietary Name: Indium In 111 Oxyquinoline
• Generic Name: Indium In-111 Oxyquinoline
• Dosage Form: Liquid
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2019-09-27
• Marketing Category: ANDA / ANDA
• Application Number: ANDA202586
• Labeler Name: BWXT ITG Canada, Inc.
• Substance Name: INDIUM IN-111 OXYQUINOLINE
• Active Ingredient Strength: 1 mCi/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72536-0920-1

1 mL in 1 VIAL, SINGLE-DOSE (72536-0920-1)

• Marketing Start Date: 2019-09-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72536-0920-1 [72536092001]

Indium In 111 Oxyquinoline LIQUID

• Marketing Category: ANDA
• Application Number: ANDA202586
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-09-27

Drug Details

Active Ingredients

Ingredient	Strength
INDIUM IN-111 OXYQUINOLINE	1 mCi/mL

OpenFDA Data

• SPL SET ID: 7dbfc0f9-0e2e-4aed-85bd-32cf7c74d402
• Manufacturer:
  • BWXT ITG Canada, Inc.
• UNII:
  • LGX9OL562T

NDC Crossover Matching brand name "Indium In 111 Oxyquinoline" or generic name "Indium In-111 Oxyquinoline"

NDC	Brand Name	Generic Name
17156-021	Indium in 111 Oxyquinoline	Indium In-111 Oxyquinoline
72536-0920	Indium In 111 Oxyquinoline	Indium In-111 Oxyquinoline