NDC 61715-050

MICONAZOLE

Miconazole

MICONAZOLE is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Kinray, Inc.. The primary component is Miconazole Nitrate.

• Product ID: 61715-050_560c02ad-d329-4458-a761-c50d8b737d69
• NDC: 61715-050
• Product Type: Human Otc Drug
• Proprietary Name: MICONAZOLE
• Generic Name: Miconazole
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-03-21
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part333C
• Labeler Name: Kinray, Inc.
• Substance Name: MICONAZOLE NITRATE
• Active Ingredient Strength: 20 mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 61715-050-01

28.4 g in 1 TUBE (61715-050-01)

• Marketing Start Date: 2013-03-22
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61715-050-01 [61715005001]

MICONAZOLE CREAM

• Marketing Category: OTC monograph final
• Application Number: part333C
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-03-22
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
MICONAZOLE NITRATE	20 mg/g

OpenFDA Data

• SPL SET ID: a44c3b24-dae2-4993-a49f-71e4eb63b231
• Manufacturer:
  • Kinray, Inc.
• UNII:
  • VW4H1CYW1K
• RxNorm Concept Unique ID - RxCUI:
  • 998483

NDC Crossover Matching brand name "MICONAZOLE" or generic name "Miconazole"

NDC	Brand Name	Generic Name
37808-928	Miconazole	miconazole nitrate
50382-050	MICONAZOLE	antifungal
61715-050	MICONAZOLE	MICONAZOLE
68016-291	Miconazole	Miconazole Nitrate
67777-316	Dynarex Antifungal Powder	Miconazole
69020-208	MakeSense	Miconazole
42669-073	Miconazole Foot Powder	Miconazole
61825-303	Oravig	Miconazole
89141-250	ORAVIG	miconazole
15071-804	Rash Relief Antifungal	Miconazole