NDC 72689-0006

FUCIDIN

Sodium Fusidate

FUCIDIN is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Oasis Trading. The primary component is Fusidate Sodium.

• Product ID: 72689-0006_7b220787-cf10-6f50-e053-2a91aa0aab6e
• NDC: 72689-0006
• Product Type: Human Otc Drug
• Proprietary Name: FUCIDIN
• Generic Name: Sodium Fusidate
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-11-21
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: OASIS TRADING
• Substance Name: FUSIDATE SODIUM
• Active Ingredient Strength: 20 mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 72689-0006-1

10 g in 1 TUBE (72689-0006-1)

• Marketing Start Date: 2018-11-21
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72689-0006-1 [72689000601]

FUCIDIN OINTMENT

• Marketing Category: unapproved drug other
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-11-21
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
FUSIDATE SODIUM	20 mg/g

OpenFDA Data

• SPL SET ID: 7b220787-cf0f-6f50-e053-2a91aa0aab6e
• Manufacturer:
  • OASIS TRADING
• UNII:
  • J7P3696BCQ

NDC Crossover Matching brand name "FUCIDIN" or generic name "Sodium Fusidate"

NDC	Brand Name	Generic Name
72689-0006	FUCIDIN	Sodium Fusidate
72988-0015	FUCIDIN	Sodium Fusidate
73442-0001	FUCIDIN	Sodium Fusidate