NDC 72988-0015

FUCIDIN

Sodium Fusidate

FUCIDIN is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Lydia Co., Ltd.. The primary component is Fusidate Sodium.

• Product ID: 72988-0015_94587991-bc94-fcfd-e053-2995a90af86a
• NDC: 72988-0015
• Product Type: Human Otc Drug
• Proprietary Name: FUCIDIN
• Generic Name: Sodium Fusidate
• Dosage Form: Ointment
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-10-08
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Lydia Co., Ltd.
• Substance Name: FUSIDATE SODIUM
• Active Ingredient Strength: 20 mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72988-0015-1

10 g in 1 TUBE (72988-0015-1)

• Marketing Start Date: 2019-10-08
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72988-0015-1 [72988001501]

FUCIDIN OINTMENT

• Marketing Category: unapproved drug other
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-10-08

Drug Details

Active Ingredients

Ingredient	Strength
FUSIDATE SODIUM	20 mg/g

OpenFDA Data

• SPL SET ID: 94586c4c-da34-47e0-e053-2a95a90a144c
• Manufacturer:
  • Lydia Co., Ltd.
• 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